CATHETER AND RETRACTABLE NEEDLE WITH PURGING SYSTEM

Abstract

Apparatus and methods pertaining to catheters used for the withdrawal of blood.

Description

FIELD OF THE INVENTION

Various embodiments of the present invention pertain to methods and apparatus for injecting medicaments into a patient and also taking a blood sample from a patient, and including embodiments having a needle retractable to within a guarded chamber after usage.

BACKGROUND OF THE INVENTION

Fluid access into the vasculature of a patient may be necessary for any of several different reasons. Such access may be necessary in order to place medicaments within the patient's circulatory system, or to remove blood or other fluids from the patient for subsequent analysis. For either reason, such access is generally established with the vasculature of the patient, such as a vein. When an infusion protocol is involved that requires periodic injections, an established fluid access site that can be repetitively used for a sequence of different injections may be required. Establishing such an access site, however, can be problematic.

Often, such access is established by a needle extending through the lumen of a catheter, such that both the tip of the needle and the tip of the catheter are located within the patient's vein. The needle is subsequently withdrawn, and the infusion or injections occur after a reservoir and tubing are attached to the luer of the catheter. In yet other situations, it is desirable to obtain blood or other bodily fluid from the patient for subsequent analysis. In such cases the blood may be drawn through a hollow needle inserted into the patient's vasculature or by connection of a blood collection reservoir to an existing, inserted catheter.

Currently, these two functions of introduction of a medicament into the patient, and withdrawal of blood from the patient, are performed in a series of multiple operations by a medical professional, using a plurality of different devices. The current requirement for multiple steps in a procedure using multiple devices provides multiple opportunities for error and multiple risks to the patient. Further, the use of multiple devices requires the clinic administrator to maintain an inventory of many separate devices. Such an inventory is not just expensive, but by itself leads to further risk to the patient if the wrong devices are stocked or used.

Yet further risks are incurred by the medical practitioner, since the devices used for introduction of a medicament or withdrawal of patient blood each can include sharp tipped needles. Since these needles are exposed to the patient's blood, there is a possibility of the medical practitioner being accidentally stuck by a used needle, with the subsequent exposure of the practitioner to the ailment of the patient.

What is needed are devices that address one or more of the aforementioned issues. Various embodiments of the present invention do this in novel and unobvious ways.

SUMMARY OF THE INVENTION

Various aspects of different embodiments of the present invention pertain to the combination of catheter placement for repeat usage, with patient fluid collection at the time of initial placement of the catheter.

Yet other embodiments include aspects directed toward safety features that protect a medical professional from being pierced accidentally by the needle used to introduce the catheter into the patient's circulatory system.

Yet other embodiments include aspects directed toward protection of the medical professional from being accidentally pierced with a needle used to place the patient's blood within a collection vial.

One aspect of the present invention pertains to an apparatus for collecting blood in a container and connecting to intravenous tubing. Some embodiments include a main body including a collection cavity adapted and configured to receive therein an end of a separate container. Other embodiments include a first hollow needle, and a second hollow needle. Still further embodiments include a catheter assembly having a body and a hollow lumen, the catheter body being adapted and configured for attachment to the intravenous tubing. The catheter body includes a one-way valve that prevents flow of blood through the lumen when the first needle is separated from the lumen.

Another aspect of the present invention pertains to an apparatus for collecting blood in a container and connecting to intravenous tubing. Some embodiments include a main body defining an interior including a collection cavity. Other embodiments include a first retractable needle having a first sharp tip, the first needle being movable from a first extended position in which the first sharp tip is exterior to the main body for insertion into a blood vessel to a second retracted position in which the first sharp tip is within the interior. Yet other embodiments include a second needle having a second sharp tip extending into the collection cavity. Still further embodiments include a catheter assembly having a body defining a hollow lumen, the catheter body being adapted and configured for attachment to the intravenous tubing. The first needle and the main body are readily separable from the catheter assembly, the first needle automatically withdrawing to the second position after separating the first needle from the catheter assembly.

Yet another aspect of the present invention pertains to a method for obtaining a sample of blood in a container from the circulatory system of a biological unit. Some embodiments include providing a hand-held device defining an interior including a collection cavity and including first and second hollow needles in fluid communication with each other, and a catheter surrounding the first needle. Yet other embodiments include inserting the first needle and the surrounding catheter into the circulatory system. Still other embodiments include placing the container in the collection cavity and inserting the second needle into the container, either before or after inserting the first needle into the circulatory system. Other embodiments include establishing fluid communication from the first needle to the container, separating the first needle and the catheter; and automatically withdrawing the first needle into the interior by the separating.

It will be appreciated that the various apparatus and methods described in this summary section, as well as elsewhere in this application, can be expressed as a large number of different combinations and subcombinations. All such useful, novel, and inventive combinations and subcombinations are contemplated herein, it being recognized that the explicit expression of each of these combinations is unnecessary.

BRIEF DESCRIPTION OF THE DRAWINGS

Some of the figures shown herein may include dimensions. Further, the figures shown herein may have been created from scaled drawings, scaled models, or from photographs that are scalable. It is understood that such dimensions, or the relative scaling within a figure, are by way of example, and not to be construed as limiting unless so stated in a claim. Persons of ordinary skill will also recognize that CAD renderings may include lines that pertain to changes in surface geometry, and not necessarily to component features.

FIG. 1 is a perspective, exploded line drawing of an apparatus according to one embodiment of the present invention.

FIG. 2 is a cross sectional view of the apparatus of FIG. 1, as represented with a drawing from a shaded CAD model, and in a first mode of operation.

FIG. 3 is a cross sectional representation of a portion of the apparatus of FIG. 2.

FIG. 4 is an enlarged cross section of a portion of the apparatus of FIG. 2.

FIG. 5 is an enlarged cross section of a portion of the apparatus of FIG. 2.

FIG. 6 is a cross sectional view of the apparatus of FIG. 2 in a second mode of operation.

FIG. 7 is a cross sectional view of the apparatus of FIG. 2 in a third mode of operation.

FIG. 8 is a cross sectional view of the apparatus of FIG. 2 in a final, used position, and ready for disposal.

FIG. 9A shows a top plan view of an apparatus according to another embodiment of the present invention.

FIG. 9B shows a side elevational view of the apparatus of FIG. 9A.

FIG. 10 is a perspective, exploded line drawing of the device of FIG. 9.

FIG. 11A is a top, partially see-thru CAD representation of the embodiment of FIG. 10, assembled, and in a first mode of operation.

FIG. 11B is a side elevational cross-sectional view of the apparatus of FIG. 11A.

FIG. 12A is a top, partially see-thru CAD representation of the embodiment of FIG. 10, assembled, and in a second mode of operation.

FIG. 12B is a side elevational cross-sectional view of the apparatus of FIG. 12A.

FIG. 13A is a top, partially see-thru CAD representation of a portion of the embodiment of FIG. 10, assembled, and in a third mode of operation.

FIG. 13B is a side elevational cross-sectional view of the apparatus of FIG. 13A.

FIG. 14A is a top, partially see-thru CAD representation of the embodiment of FIG. 10, assembled, and in a final, used position, and ready for disposal.

FIG. 14B is a side elevational cross-sectional view of the apparatus of FIG. 14A.

FIGS. 15A, 15B, and 15C are top perspective, top plan, and cross sectional line drawings, respectively, of the luer body of FIG. 10.

FIGS. 16A and 16B are top rear and top front perspective line drawings, respectively, of the holder top of FIG. 10.

FIGS. 16C, 16D, and 16E are top plan, side elevational, and cross sectional line drawings, respectively, of the apparatus of FIG. 16A.

FIGS. 17A, 17B, and 17C are top rear, side elevational, and cross sectional line drawings, respectively, of a portion of the needle assembly of FIG. 10.

FIGS. 18A and 18B are top rear and top front perspective line drawings, respectively, of the collection adapter body of FIG. 10.

FIGS. 18C and 18D are side elevational and side cross sectional line drawings, respectively, of the apparatus of FIG. 18A, with FIG. 18D being a cross sectional representation of FIG. 18C as taken along the centerline of FIG. 18C.

FIGS. 19A and 19B are top rear and top front perspective line drawings, respectively, of the sliding disc member of FIG. 10.

FIGS. 19C and 19D are side elevational and top plan views, respectively, of the apparatus of FIG. 19A, with FIG. 19D being the view looking down from line 19D-19D of FIG. 19C.

FIGS. 19E and 19F are front end and rear end views, respectively, of the apparatus of FIG. 19A.

FIGS. 20A and 20B are rear elevational and top rear perspective line drawings, respectively, of the holder body of FIG. 10.

FIGS. 20C and 20D are side elevational and cross sectional line drawings, respectively, of the apparatus of FIG. 20A.

FIGS. 21A and 21B are top rear and top front perspective line drawings, respectively, of an alternative to the sliding disc member of FIG. 10.

FIGS. 21C and 21D are side elevational and top plan views, respectively, of the apparatus of FIG. 21A, with FIG. 21D being the view looking down from line 21D-21D of FIG. 21C.

FIGS. 21E and 21F are front end and rear end views, respectively, of the apparatus of FIG. 21A.

FIG. 22A is an exploded view of a portion of an apparatus 320 according to another embodiment of the present invention.

FIG. 22B is an end view of a portion of an apparatus 320 according to another embodiment of the present invention.

FIG. 22C is one alternative to the embodiment of FIG. 22B.

FIG. 22D shows a cross section of a portion of apparatus 320 prior to retraction of the first needle assembly.

FIG. 22E shows the apparatus of FIG. 22D after the needle body has retracted and contacted an internally sliding component, and prior to full retraction of the first needle.

FIG. 22F shows a cross section of a portion of an alternative apparatus 320-2 prior to retraction of the first needle assembly.

FIG. 23A is a side elevational cross sectional representation of a portion of an apparatus 420 according to another embodiment of the present invention.

FIG. 23B shows a cross section of a portion of apparatus 420 after initial retraction and prior to full retraction of the first needle assembly.

FIG. 23C shows the apparatus of FIG. 22D after the needle body has fully retracted.

FIG. 24A is an end elevational view of a portion of an apparatus 520 according to another embodiment of the present invention.

FIG. 24B shows a cross section of a portion of apparatus 520 after initial retraction and prior to full retraction of the first needle assembly.

FIG. 24C shows the apparatus of FIG. 22D after the needle body has fully retracted and contacted an internally sliding component.

FIG. 26 shows a cross sectional view of a portion of an apparatus according to another embodiment of the present invention.

FIG. 27a presents a close up view of a portion of the apparatus of FIG. 26 shown in a configuration permitting the exhaust of gas and blood to a flash chamber.

FIG. 27b shows the apparatus of FIG. 27a after occlusion of the filter with blood.

FIG. 28A shows a schematic representation of a flow system corresponding to FIG. 27a.

FIG. 28b shows a schematic representation of a flow system corresponding to FIG. 27b.

ELEMENT NUMBERING

The following is a list of element numbers used with all of the embodiments, and at least one noun used to describe that element. The “X” for all of these numbers is replaced with a number (0 or greater) in the text and drawings of this application. Consistent with statements made elsewhere in this specification, these various element numbers are used among multiple embodiments, and aspects of a particular element stated for one embodiment can be applied to the same element number in a different embodiment, except as shown and described differently, and as would be understood by a person of ordinary skill in the art. It is understood that none of the embodiments disclosed herein are limited to these nouns, and these element numbers can further include other words that would be understood by a person of ordinary skill reading and reviewing this disclosure in its entirety.

X10	collection vessel	X34	luer body
X11	first position	X35	locking feature
X12′	movement toward second position	X36	eyelet
X12	second position	X37	eyelet receptacle
X20	apparatus	X38	valve, 1-way or 2-way
X21.1	main body	X39	valve receptacle
X21.2	collection cavity	X40	needle assembly
X22	cap	X42	cannula, sharp tipped
X24	holder top	X44	a adapter
.1	collection valve guide	X45	flat or flattened area; groove
.2	collection valve slot	X46	spring
.3	interior	.1	spring guide
X25	window	.2	ridges
X26	holder body	.3	recess
X27	cylindrical receptacle; wall	X47	centerline; axis
.1	distal guide and stop; groove	X48	tube
.2	2nd complementary feature	.1	tube guide
.3	proximal guide and stop; groove	.2	tube port
.4	pocket	.3	tube port
X28	fingers	.4	tube holder
X29	collector aperture	X50	collection valve assy.
X30	IV catheter assy	X51	locking tabs; guiding ear
X32	flexible lumen	X52	cannula
.1	First flowpath
.2	Inlet
.3	outlet
X53	Second sharp tipped needle
.1	First flowpath
X54	b adapter body
X55	body guided member
X56	sheath
.1	sheath coupling
X57	centerline; axis
X58	filter
.1	Before contact with blood
.2	After contact with blood
X59	filter receptacle
.1	Second flowpath
.2	Inlet
.3	outlet
X60	sliding disk member
X61	leg
X62	protrusion; 1st complementary
	feature
X63	cover
X64	flexible hinge member; ear
X65	shoulder wings
X66	cannula aperture
X70	damping element
X71	bumper
a	attachment surface
b	contact surface
X72	rub strip
a	attachment surface
b	contact surface
X80	One-way valve
.1	open
.2	closed
X81	Flexible valve member; movable
	valve member
X82	screen

DESCRIPTION OF THE PREFERRED EMBODIMENT

For the purposes of promoting an understanding of the principles of the invention, reference will now be made to the embodiments illustrated in the drawings and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended, such alterations and further modifications in the illustrated device, and such further applications of the principles of the invention as illustrated therein being contemplated as would normally occur to one skilled in the art to which the invention relates. At least one embodiment of the present invention will be described and shown, and this application may show and/or describe other embodiments of the present invention. It is understood that any reference to “the invention” is a reference to an embodiment of a family of inventions, with no single embodiment including an apparatus, process, or composition that should be included in all embodiments, unless otherwise stated. Further, although there may be discussion with regards to “advantages” provided by some embodiments of the present invention, it is understood that yet other embodiments may not include those same advantages, or may include yet different advantages. Any advantages described herein are not to be construed as limiting to any of the claims. The usage of words indicating preference, such as “preferably,” refers to features and aspects that are present in at least one embodiment, but which are optional for some embodiments.

The use of an N-series prefix for an element number (NXX.XX) refers to an element that is the same as the non-prefixed element (XX.XX), except as shown and described. As an example, an element 1020.1 would be the same as element 20.1, except for those different features of element 1020.1 shown and described. Further, common elements and common features of related elements may be drawn in the same manner in different figures, and/or use the same symbology in different figures. As such, it is not necessary to describe the features of 1020.1 and 20.1 that are the same, since these common features are apparent to a person of ordinary skill in the related field of technology. Further, it is understood that the features 1020.1 and 20.1 may be backward compatible, such that a feature (NXX.XX) may include features compatible with other various embodiments (MXX.XX), as would be understood by those of ordinary skill in the art. This description convention also applies to the use of prime (′), double prime (″), and triple prime (′″) suffixed element numbers. Therefore, it is not necessary to describe the features of 20.1, 20.1′, 20.1″, and 20.1″ that are the same, since these common features are apparent to persons of ordinary skill in the related field of technology.

Although various specific quantities (spatial dimensions, temperatures, pressures, times, force, resistance, current, voltage, concentrations, wavelengths, frequencies, heat transfer coefficients, dimensionless parameters, etc.) may be stated herein, such specific quantities are presented as examples only, and further, unless otherwise explicitly noted, are approximate values, and should be considered as if the word “about” prefaced each quantity. Further, with discussion pertaining to a specific composition of matter, that description is by example only, and does not limit the applicability of other species of that composition, nor does it limit the applicability of other compositions unrelated to the cited composition.

Various references may be made to one or more processes, algorithms, operational methods, or logic, accompanied by a diagram showing such organized in a particular sequence. It is understood that the order of such a sequence is by example only, and is not intended to be limiting on any embodiment of the invention.

This document may use different words to describe the same element number, or refer to an element number in a specific family of features (NXX.XX). It is understood that such multiple usage is not intended to provide a redefinition of any term herein. It is understood that such words demonstrate that the particular feature can be considered in various linguistical ways, such ways further not necessarily being additive or exclusive.

Various embodiments of the invention disclosed herein combine the basic elements of both an IV catheter and a blood collector and then expands upon those features resulting in a fully automatic/passive safety product that seamlessly shields the user against needle stick injuries in one simple step. Immediately upon separation of the catheter luer from the main body, both cannula sharps are simultaneously and automatically shielded within the collection holder. This renders the device unusable and safe for proper disposal. As used herein, the term “proximal” refers to proximity to the user, and with regards to FIG. 2 or 9, to the right of the drawing. The word “distal” refers to a direction generally opposite of the proximal direction.

FIG. 1 presents an exploded view of an apparatus 20 according to one embodiment of the present invention. Apparatus 20 provides a single device that can be used as part of a catheter for the intravenous delivery of medicaments, but also provide an interface through which the patient's blood can be collected. In still further embodiments, the apparatus includes a needle that is useful for puncturing a vein of a patient, and also for providing a flow of the patient's blood into a separate collection vessel such as a standard collection tube (not shown).

FIG. 1 shows an apparatus 20 having an IV catheter 30, needle assembly 40, collection valve 50, and latching disk 60. The catheter 30, needle 40, valve 50, and disk 60 are contained within a cap 22, holder top 24, and holder body 26.

Apparatus 20 can be seen in a side elevational cross sectional view in FIG. 2. The holder top 24 and holder body 26 in one embodiment are molded plastic pieces that are joined together by any suitable process, including as examples, by way of snap fit, by adhering with a glue, by ultrasonic welding, or the like. Although holder top 24 and holder body 26 are shown as two separate pieces, it is understood that various embodiments of the present invention contemplate these two components being combined into a single main body 21.1, and still further contemplates those other embodiments in which the various structural features of holder top 24 and holder body 26 are redistributed among two or more different separate pieces, but which still function as a main body 21.1 when assembled. The catheter assembly 30, needle assembly 40, and collection valve assembly 50 are all preferably supported by the holder top 24, as will be described.

FIG. 2 shows a view of apparatus 20 in which protective cap 22 has been removed. It is understood that cap 22 provides for safe handling of the sterile, exposed needle 42 and catheter 32 during storage and handling. The opened proximal end of cap 22 fits over the distal-most end of holder top 24 in a manner that provides not only for safe handling and storage, but also for easy, ready removal by a medical professional. Preferably, cap 22 covers lumen 32 and luer 34.

Placed on the distal-most end of holder top 24 is an intravenous catheter assembly 30. Assembly 30 includes a hollow luer body 34 that includes a flexible lumen 32 extending in a distal-direction. Lumen 32 is preferably attached to an inner surface of luer body 34 by way of an eyelet 36. Luer body 34 also supports an internal one-way valve 38 that is located generally in the middle of the length of body 34. In some embodiments, valve 38 is a 1-way valve, whereas in other embodiments it is a 2-way valve. Preferably, valve 38 permits cannula 42 to be extended through the valve dome, without leakage. Upon withdrawal of cannula 42, the dome of valve 38 substantially seals to a fluid-tight state.

The proximal end of body 34 includes an inner diameter that establishes a friction fit over a pair of forward-extending fingers 28 that are part of holder top 24 (shown in FIG. 4). In some embodiments, luer body 34 also includes a plurality of ridges on one or more outer surfaces that assist the medical practitioner in handling of catheter assembly 30.

FIGS. 2 and 4 include cross sectional views of a needle assembly 40. Needle assembly 40 preferably includes a beveled, sharp-tipped needle 42 that is fixed to the internal surfaces of a shuttling adapter 44. Cannula 42 is adapted and configured to extend within flexible lumen 32 of catheter 30. The tip of cannula 42 extends beyond the end of flexible lumen 32. During insertion of needle 42 and lumen 32 into the vein of a patient, needle 42 provides a stiffening function that maintains the cylindrical shape of lumen 32, preventing buckling of lumen 32 during insertion of the needle 42 and catheter 30 into the vein of the patient.

As best seen in FIG. 4, needle assembly 40 further includes a spring 46 that is located between opposing, facing shoulders of adapter 44 and holder top 24. FIG. 4 shows needle assembly 40 inserted fully within catheter assembly 30, with the resultant maximum compression of spring 46. Preferably, spring 46 is a coil spring, although it is appreciated that various devices and methods can be used to bias apart adapter 44 and the forward shoulder of holder top 24. It can also be seen in FIG. 4 that cannula 42 extends through the distal-most end of valve 38, and thus provides fluid communication from the tip end aperture of needle 42, to the proximal-most opened end of adapter body 44.

Referring to FIG. 4, a disk leg 61 operating as a guide for adapter 44 can be seen (leg 61 preferably not being engaged with adapter 44). A first latching mechanism between disk 60 and holder top 24 establishes the relative locations of needle assembly 40 and disk 60. A second latching mechanism establishes the relative positions of disk 60 and holder body 26. Disk 60 sits in a relaxed position between the holder top and holder body with a slight interference fit. In a manner that will be described later, leg 61 of disk 60 maintains radial alignment within the holder body 24 and acts as a guide to needle assembly 40 in a forwardmost position, with spring 46 under near-maximum compression, during a first mode of operation of apparatus 20.

FIG. 5 shows an enlarged sectional view of a portion of apparatus 20. A latching disk 60 can be seen located within a generally cylindrical aperture 29 of holder body 26. Disk 60 is preferably a single, molded piece having a forwardly-extending leg. Various features of disk 60 are adapted and configured to provide a first latching between disk 60 and retractable need assembly 40, and a second latching between disk 60 and either holder top 24 or holder body 26.

Collection valve assembly 50 is attached to internal support ribs of holder top 24. Disk 60 includes a small, central aperture that loosely fits around an outer diameter of a shoulder of adapter 54. Thus, disk assembly 60 is free to move relative to adapter body 54, and body 54 is held fixed by holder top 24. A flexible tube 48 provides fluid communication from adapter 44 and cannula 42 to one end of adapter body 54.

Referring briefly to FIG. 2, it can be seen that adapter 54 establishes a centerline 57 generally within the center of chamber 21.2 of holder body 26. Adapter body 44 and cannula 42 establish a second centerline 47 that is generally parallel to, and offset from, centerline 57. However, it is understood that yet other embodiments of the present invention contemplate relative arrangements of the centerlines of needle assembly 40 and collection valve assembly 50, including non-parallel arrangements (in which centerline 57 and aperture 29 of holder body 26 would be angled upward, away from the patient, referring to FIG. 2) and also those embodiments in which centerlines 47 and 57 are not offset (such as when the two axes are generally aligned).

Referring again to FIG. 5, it can be seen that adapter 54 supports a cannula 52 that extends rearward toward the proximal opening 29 of holder body 26. A conical barb at the proximal end of adapter body 54 further support a flexible sheath 56 that generally surrounds and seals cannula 52 to adapter body 54. Preferably, sheath 56 is fabricated from a flexible material, such as a silicone rubber, and can therefore easily be compressed and collapsed around cannula 52. The proximal-most end of cannula 52 preferable includes a beveled, sharp tip for puncturing a collection vessel, as will be described later.

FIG. 5 further shows that adapter body 54 supports a porous filter 58 that provides a purging function for the interior volume of cannula 42, adapter body 44, tube 48, and adapter body 54. The proximal end of disk 60 includes a protrusion 62 that is shown in FIG. 6 as being held against a forward ledge of holder body 26.

Apparatus 20 operates in several different modes. FIG. 1 is an exploded view of a storage mode of operation, in which catheter assembly 30 is located at the distal-most end of holder top 24, with full compression of spring 46. Further, in this storage mode, sheath 56 is unpunctured, and maintains the sterility of the internal flowpath of assembly 20.

FIG. 2 represents apparatus 20 in a first mode of operation. Cap 22 has been removed, exposing the sharp tip of cannula 42 and the exterior of flexible lumen 32. The medical practitioner has access to hold the exterior of luer body 34, as well as the ability to hold the exterior of holder top 24 and holder body 26. The medical practitioner places the sharp tip of cannula 40 relative to a vein of a patient, and inserts the cannula 42 and flexible lumen 32 within the vein of the patient.

In a second mode of operation, the medical practitioner can bring a standard collection vessel 10 (not shown) through aperture 29 and into the opened proximal chamber 21.2 of holder body 26. The proximal end of body 26 includes a generally cylindrical chamber 21.2. The interior dimensions of the proximal end of holder body 26 are slightly greater than the outer diameter of the collection vessel. Therefore, the collection vessel enters aperture 29, and the face of the collection vessel can be brought into contact with the proximal end of sheath 56.

Preferably, the end of the collection vessel 10 is soft enough such that the medical practitioner can push the collection vessel against sheath 56 and the sharp tip of cannula 52. By continuing to push the collection vessel toward adapter 54, the sharp tip of cannula 52 penetrates the end of collection vessel 10, and enters the interior of the collection vessel. However, the flexible sheath 56 does not enter the collection vessel, and instead is compressed in buckling along cannula 52 and toward adapter body 54.

Once the tip of cannula 52 extends within the empty volume of collection vessel 10, fluid communication is established from the interior of the collection vessel through cannula 52 and adapter body 54, through tube 48, and into the interior flow passage of needle assembly 40. Since needle assembly 40 is exposed to blood within the patient's vein, blood can begin to flow through needle assembly 40 and tube 48, through collection valve assembly 50, and into collection vessel 10.

In order to prevent any hydraulic lockup, the interior of collection vessel 10 can be established at a pressure less than the pressure of the blood within the vein, or a suitable fluid induction device can be used. Still further, any trapped air within needle assembly 40, tube 48, and valve assembly 50 can escape through porous filter 58. However, filter 58 is preferably of a type in which the porosity of the filter is maintained only so long as the filter does not contact blood (such as a POREX® material). Upon contact with the blood, the filter media loses porosity, such that there can be no further leakage of either trapped air or blood through the filter. As blood flows through tube 48, it can be seen by the medical practitioner through a transparent window 25 within holder top 24.

The medical practitioner maintains collection vessel 10 within holder body 26 and in fluid communication with the vein of the patient until sufficient blood has been collected. Multiple collection vials maybe used. After the medical professional has collected sufficient blood, the compression is relieved and the collection vessel 10 is withdrawn. The adapter 44 assembly still remains in a distal position, under spring load, until the luer assembly 30 has separated from the Holder Top 24. The relationship between the luer body 34, holder top legs 28 and adapter 44 receiving flats 45 prevent movement. Once the user advances the catheter luer assembly in a distal direction beyond legs 28, there is nothing to prevent them from flexing outward. This outward flexing releases adapter 44 so it can move in a proximal direction, retracting toward the proximal end of holder body 26. Needle assembly 40 can move rearward toward a receiving pocket on the end of disk 60. Both disk 60 and needle assembly 40 therefore move toward the proximal end of the body holder. The beginnings of this movement can be first seen in FIG. 6. The full seating of the needle assembly in the receiving pocket of disk 60 can be seen in FIG. 7 Cannula 42 of needle assembly 40 retracts within flexible lumen 32 of catheter assembly 30. However, the medical practitioner advances the catheter assembly 30 into the patient's vein, with the result that lumen 32 remains in fluid communication with the patient's vein. However, as needle assembly 40 retracts, the end of the needle assembly retracts past flexible valve 38, which acts as a one-way valve, and thereby closes and prevents any escape of the patient's blood.

FIGS. 7 and 8 show the remaining retraction of needle assembly 40 within holder body 26. As the assembly of the disk and needle retract, tube 48 begins to extend. FIG. 7 shows the completed and full retraction of needle assembly 40 relative to disk 60. FIG. 8 shows the completed and full retraction of the disk relative to holder 26. The aft face of disk 60 is biased by spring 46 to sit against a ledge or shoulder surrounding aperture 29 of holder body 26 and locks into place preventing any further movement. Tube 48 is shown in its position of maximum extension from the end of adapter 44 to the end of adapter 54. The sharp tip of cannula 42 is fully contained within holder top 24.

In some embodiments, the relationship between adapter 44 and disk 60 is generally for guiding disk 60 to its full proximal position. Various embodiments do not include features that pre-stage activation upon insertion of a collection Tube 10. The disk 60 statically stays positioned in the holder top 24 by a simple interference fit having a reverse draft. Multiple collection tubes can be used without activation since activation (retraction of the needle assembly 40 and disk 60) does not occur until the catheter luer assembly 30 has separated from the holder 24.

FIGS. 9-20 pertain to an apparatus 120 according to another embodiment of the present invention. FIG. 9A and FIG. 9B show top and side external views, respectively, of device 120. A main body 121.1 has a protective cap 122 on one end, and an aperture 129 defined on the opposite end, the aperture being adapted and configured to accept a collection vessel. Although what will be shown and described is an embodiment configured to accept a vessel such as an evacuated, cylindrical vessel, the present invention further contemplates those embodiments in which the aperture is adapted and configured to accept any shape, size, or type of collection vessel, and further included those embodiments adapted and configured to accept tubing-like components that are in fluid communication with a collection reservoir.

FIG. 10 presents an exploded view of an apparatus 120 according to one embodiment of the present invention. Apparatus 120 provides a single device that can be used as part of a catheter for the intravenous delivery of medicaments, but also provide an interface through which the patient's blood can be collected. In still further embodiments, the apparatus includes a needle that is useful for puncturing a vein of a patient, and also for providing a flow of the patient's blood into a separate collection vessel such as a standard collection tube (not shown).

FIG. 10 shows an apparatus 120 having an IV catheter 130, needle assembly 140, collection valve 150, and latching disk 160. The catheter 130, needle 140, valve 150, and disk 160 are contained within a cap 122, holder top 124, and holder body 126.

Apparatus 120 can be seen in a top elevational view in FIG. 11A and a side elevational cross sectional view (taken along the centerline of FIG. 11A) in FIG. 11B. The holder top 124 and holder body 126 in one embodiment are molded plastic pieces that are joined together by any suitable process, including as examples, by way of snap fit, by adhering with a glue, by ultrasonic welding, or the like. The catheter assembly 130, needle assembly 140, and collection valve assembly 150 are all preferably supported by the holder top 124, as will be described.

FIGS. 11A and 11B show views of apparatus 120 in which protective cap 122 has been removed. It is understood that cap 122 provides for safe handling of the sterile, exposed needle 142 and catheter 132 during storage and handling. The opened proximal end of cap 122 fits over the distal-most end of holder top 124 in a manner that provides not only for safe handling and storage, but also for easy, ready removal by a medical professional. Preferably, cap 122 covers lumen 132 and luer body 134, and the tip of cannula 142.

Placed on the distal-most end of holder top 124 is an intravenous catheter assembly 130. Assembly 130 includes a hollow luer body 134 that includes a flexible lumen 132 extending in a distal-direction. Lumen 132 is preferably attached to an inner surface of luer body 134 by way of an eyelet 136. Luer body 134 also supports an internal valve 138 within a receptacle 139 that is located generally in the middle of the length of body 134 (luer body 134 also being shown in FIG. 15). The proximal end of body 134 includes an inner diameter that establishes a friction fit over a pair of forward-extending fingers 128 that are part of holder top 124 (also shown in FIGS. 14A and 14B). In some embodiments, luer body 134 also includes a plurality of ridges on one or more outer surfaces that assist the medical practitioner in handling of catheter assembly 130. The placement of luer body 134 over fingers 128 causes the tips of these fingers to be pressed firmly within corresponding flats 145 of body 144 (as seen in FIG. 17). The inner surface of luer body 134 fits over fingers 128 and compresses them into flats 145 so as to firmly hold needle assembly 140 in place, and able to resist a force exerted on needle assembly 140 by spring 146 (as will be discussed later). Luer body 134 includes one or more locking features 135 that are adapted and configured for connection to another medical device.

FIG. 16 show various views of a portion of a main body according to one embodiment of the present invention. In this embodiment, the main body includes a holder top 124 that provides a variety of functions with a variety of different features. These functions and features will be described, but it is understood that the present invention contemplates those embodiments in which one or more of these functions and features are not included.

Holder top 124 includes a distal end having a pair of distally extending fingers 128 that provide for capture of needle assembly 140 as discussed herein. The proximal end of holder top 124 defines an aperture that is adapted and configured to receive therein the distal end of the holder body 126. Further, the open proximal end of holder top 124 includes a pair of distal guide/stop grooves 127.1 arranged on generally opposite sides. These grooves 127.1 coact with corresponding ears 164 of sliding disk member 160 as will be described later. The open end of holder top 124 further includes a guiding feature 127.2 that is generally complementary in shape to a corresponding guiding feature 162 of sliding disk member 160, as will be discussed later.

Holder top 124 includes an outer shape adapted and configured to provide a hand hold for the medical professional. As best seen in FIG. 16B, holder top 124 has a width that decreases in the distal direction, and further has a height that decreases in the distal direction. This curving shape, which reduces from proximal to distal end, provides a secure hold of apparatus 120 within the hand and fingers of a medical professional.

Holder top 124 receives within it a collection valve assembly 150, this assembly 150 being seen in side view on FIGS. 11B, 12B, 13B, and 14B. Holder top 124 includes a guide 124.1 that receives within it a correspondingly-shaped guided member 155 of body 154 (as seen in FIGS. 18A and 18B). This guiding chamber 124.1 extends generally above needle assembly 140 and leg 161.

In apparatus 120, holder top 124 provides for the internal placement of a needle assembly 140 and collection valve assembly 150 having cannula axes 147 and 157, respectively, that are generally parallel and vertically displaced from one another (as best in FIG. 11B). However, other embodiments of the present invention are not so limited. For example, yet other embodiments include a collection valve assembly having a cannula axis that is tilted relative to the cannula axis of the first needle, such that the collection cavity 121.2 is tilted upward, toward the face of the user during usage. Such embodiments further contemplate needle assemblies 140 that retract generally into the interior of main body 121.2, but not necessarily into the collection cavity. Still further, although FIGS. 11A and 11B show cannula axes 147 and 157 being parallel and displaced, yet other embodiments contemplate the axes being coincident. In such embodiments, it is contemplated that the first and second cannulas 142 and 152 can be unitary, such that both the needle assembly 140 and the cannula 152 retract from a first, ready-to-use position to a second, used position, after removal of catheter assembly 130 or actuation of some other retraction-causing feature.

Referring to FIGS. 16C and 16E, it can be seen that holder top 124 includes a slot 124.2 that is adapted and configured to receive within it a corresponding guiding ear or locking tab 151 of adapter body 154 (as best seen in FIGS. 18A and 18B). The coaction of slot 124.2 and tab 151 provides for alignment of holder body 154 relative to holder top 124 (and therefore alignment with needle assembly 140). Referring to FIG. 18B, it can be seen that tab 151 in some embodiments provides a unidirectional, snap fit. Tab 151 has an angled, expanding leading edge to assist in temporary expansion of guide 124.1 during assembly, yet also includes a squared-off trailing edge that makes holder body 154 resistant to accidental disassembly and removal, the outermost diametral portions of ear 151 being in interference with portions of body 124 after the entire tab 151 is contained within slot 124.2, such that the temporarily expanded holder top 124.1 snaps back into place.

FIG. 11B shows a cross sectional view of a needle assembly 140. Needle assembly 140 preferably includes a beveled, sharp-tipped needle 142 that is fixed to the internal surfaces of a shuttling adapter 144. Cannula 142 is adapted and configured to extend within flexible lumen 132 of catheter 130. The tip of cannula 142 extends beyond the end of flexible lumen 132. During insertion of needle 142 and lumen 132 into the vein of a patient, needle 142 provides a stiffening function that maintains the cylindrical shape of lumen 132, preventing buckling of lumen 132 during insertion of the needle 142 and catheter 130 into the vein of the patient.

FIG. 17 show additional views of the adapter body 144 of needle assembly 140. Body 144 includes a front cylindrical cavity to which cannula 142 is attached, and which establishes a centerline 147 of cannula 142. Body 144 further includes a plurality of ridges 146.1 that assist in aligning and guiding an end of spring 146 (as can be seen in FIG. 11B). Body 144 further includes a shoulder 146.2 that receives an end 148.2 of spring 146, and against which spring 146 exerts a load.

The proximal end of body 144 is adapted and configured to receive within it an end of tube 148. FIG. 17C shows an internal cylindrical cavity 148.2 that receives the end of tube 148. As tube 148 exits from body 144, the tube makes a right angle turn through tube holding feature 148.4. It can be seen that feature 148.4 includes a generally semi-cylindrical shape that receives the outer diameter of the tube. However, this cylindrical shape is opened to the proximal end of body 144 by a V-shaped pair of upper and lower walls. As best seen in FIG. 17C, these angularly-shaped walls narrow down to a minimum distance that is large enough to permit tube 148 to be squeezed past these walls during assembly, but small enough to prevent the assembled and inserted, right-angled tube from escaping the semi-cylindrical aperture. The placement of tube holding feature 148.4 on a side of body 144 provides for less impedance by tube 148 on the retraction on needle assembly 140, by placing the sharpest turn radius of tube 148 held firmly within body 144. Therefore, very little of the spring force is consumed by any requirement to make a sharp bend in tube 148 as it retracts (referring to FIGS. 13A and 14A).

As best seen in FIG. 11B, needle assembly 140 is acted upon by a spring 146 that is located between the shoulder 146.2 of adapter 144 and a recess 146.3 of holder top 124 (as best seen in FIG. 16E). FIG. 4 shows needle assembly 140 inserted fully within catheter assembly 130, with the resultant maximum compression of spring 146. Preferably, spring 146 is a coil spring, although it is appreciated that various devices and methods can be used to bias apart adapter 144 and the forward shoulder of holder top 124. It can also be seen in FIG. 4 that cannula 142 extends through the distal-most end of valve 138, and thus provides fluid communication from the tip end aperture of needle 142, to the proximal-most opened end of adapter body 144. Tube 148 continues the path of fluid communication from adapter body 144 to adapter body 154, as will be discussed later.

Some embodiments of the present invention further include a sliding member 160 that can provide a plurality of functions with an apparatus 120. As one example, and as best seen in FIGS. 11A and 11B, sliding member 160 includes a cover 163 that includes an aperture 166 through which second needle 152 extends. Further, FIG. 11A shows that extending distally and on the bottom side of sliding member 160 is a leg 161 that fits generally underneath and guides the distal end of needle assembly 140. Still further, sliding member 160 includes a pair of outwardly extending ears 164 that coact with the main body to prevent sliding member 160 from moving distally forward from the first position 111, shown in FIGS. 11A and 11B. Sliding member 160 further defines a pocket 127.4 that provides placement of needle assembly 140 in both the partially retracted and fully retracted states (as seen in FIGS. 13B and 14B, respectively). Still further, the ears 164 of sliding disk 160 coact with main body 121.1 to prevent distal-direction movement of the cover 163 in the final, used configuration (as shown in FIGS. 14A and 14B).

Referring to FIGS. 11B and 19D, a disk leg 161 operating as a guide for adapter 144 can be seen (leg 161 preferably not being engaged with adapter 144). A first latching mechanism between disk 160 and holder top 124 establishes the relative locations of needle assembly 140 and disk 160 in the first, ready to use position 111. A second latching mechanism establishes the relative positions of disk 160 and holder body 126, in the final, used second position 112. Disk 160 sits in a relaxed position between the holder top and holder body with a slight interference fit. In a manner that will be described later, leg 161 of disk 160 maintains radial alignment within the holder body 124 and acts as a guide to needle assembly 140 in a forwardmost position 111, with spring 146 under near-maximum compression, during a first mode of operation of apparatus 120.

Sliding member 160 is also shown in FIG. 19. Sliding member 160 includes a disk-shaped proximal end 163 that includes within it a generally centered aperture 166. A pair of flexibly hinged members or ears 164 extends generally outward on opposing sides of member 160. A leg 161 extends distally from the inner face of cover 163, and has a generally curved shape to it as seen in FIGS. 19E and 19F. Sliding member 160 further includes a semi-cylindrical wall 127 that defines therein a pocket 127.4.

Flexible ears 164 coact with complementary-shaped distal and proximal guide/stop grooves 127.1 and 127.3, respectively. These guide/stop grooves include a short length in the axial direction adapted and configured to receive the distal end of the ear, and provide guidance of the ear during sliding contact. The guide/stop grooves further include a distalmost endwall that is adapted and configured to coact with the corresponding ears to prevent distal motion beyond a first distalmost position (when the apparatus 120 is ready to be used) and a second distalmost position (after the device has been used, and the collection container withdrawn).

Distal guide/stop 127.1 can be seen in FIGS. 16A, 16B, and 16C. Proximal guide/stop 127.3 can be seen formed into holder body 126 in FIGS. 20B, 20C, and 20D. Ears 164 of sliding member 160 coact with proximal grooves 127.1 to limit the distalmost travel of member 160 in the first position (as can be seen in FIG. 12A). However, ears 164 are adapted and configured to not interfere with the sliding motion of member 160 from the first position toward the second position. In the fully extended and final position (as seen in FIG. 14A), ear 164 coacts with groove 127.3 to stop movement of member 160 in a distal direction after sliding member 160 is fully in the second position 112.

Sliding member 160 further includes a guiding feature 162 that has a shape complementary to a guiding feature 127.2, the latter being shown in FIG. 20B and FIG. 16A. Complementary-shaped features 162 and 127.2 coact to guide sliding member 160 within the main body 121.1 of apparatus 120 (as also seen in FIG. 14B). The guiding feature 162 in some embodiments fulfills a second function as a leg 161 that fits under and generally close to the bottom of adapter body 144 (as seen in FIGS. 11B and 12B). The curved shape of this leg further assists in guiding adapter body 144 into pocket 127.4, as needle assembly 144 retracts from the first position 111 into the second (and intermediate) position 112′ (as seen in FIG. 13B). It is understood that in some embodiments the needle body-guiding function of leg 161 and the sliding member-guiding function (relative to main body 121.1) of guiding feature 162 can be accomplished simultaneously with the tongue-like structure shown in FIG. 19B. However, yet other embodiments contemplate configurations of the sliding member 160 in which these two guiding functions are performed separately on a sliding member, and still further contemplate those embodiments in which these functions are accomplished not on the sliding member but on other structure of the apparatus 120.

FIGS. 11 and 12 show views of a portion of apparatus 120. A latching disk 160 can be seen located within a generally cylindrical aperture 129 of holder body 126. Disk 160 is preferably a single, molded piece having a forwardly-extending leg. Various features of disk 160 are adapted and configured to provide a first latching between disk 160 and retractable need assembly 140, and a second latching between disk 160 and either holder top 124 or holder body 126.

Collection valve assembly 150 is attached to internal support ribs of holder top 124. Disk 160 includes a small, central aperture that loosely fits around an outer diameter of a shoulder of adapter 154. Thus, disk assembly 160 is free to move relative to adapter body 154, and body 154 is held fixed by holder top 124. A flexible tube 148 provides fluid communication from adapter 144 and cannula 142 to one end of adapter body 154.

Referring briefly to FIG. 11B, it can be seen that adapter 154 establishes a centerline 157 generally within the center of chamber 121 of holder body 126. Adapter body 144 and cannula 142 establish a second centerline 147 that is generally parallel to, and offset from, centerline 157. However, it is understood that yet other embodiments of the present invention contemplate relative arrangements of the centerlines of needle assembly 140 and collection valve assembly 150, including non-parallel arrangements (in which centerline 157 and aperture 129 of holder body 126 would be angled upward, away from the patient, referring to FIG. 2) and also those embodiments in which centerlines 147 and 157 are not offset (such as when the two axes are generally aligned).

It can be seen that adapter 154 supports a cannula 152 that extends rearward toward the proximal opening 129 of holder body 126. A conical barb at the proximal end of adapter body 154 further support a flexible sheath 156 that generally surrounds and seals cannula 152 to adapter body 154. Preferably, sheath 156 is fabricated from a flexible material, such as a silicone rubber, and can therefore easily be compressed and collapsed around cannula 152. The proximal-most end of cannula 152 preferable includes a beveled, sharp tip for puncturing a collection vessel, as will be described later.

Adapter body 154 supports a porous filter 158 that provides a purging function for the interior volume of cannula 142, adapter body 144, tube 148, and adapter body 154. The proximal end of disk 160 includes a protrusion 162 that is shown in FIG. 6 as being held against a forward ledge of holder body 126.

FIG. 18 show various views of an adapter body 154 according to one embodiment of the present invention. Body 154 includes a proximal end having a coupling feature 156.1 that is inserted into, and seals around, the open end of flexible sheath 156. Adjacent to coupling 156.1 is a cylindrical collar that closely fits within aperture 166 of sliding disk member 160. Adjacent to this centering collar is a receptacle 159 that receives within it filter 158. Referring to FIG. 18D, it can be seen that receptacle 159 includes an aperture in the bottom that provides fluid communication to the flowpath extending along centerline 157, this flowpath beginning at the tip of needle 142 and extending to the tip of needle 152, and further into the collection reservoir when the collection reservoir is in place. By way of this secondary flowpath to filter 158, any trapped air within the main flowpath can be released through the filer. Once the filer cavity fills with blood, the blood coacts with the filter media to block any outward flow from receptacle 159. FIG. 18D also shows that the flowpath upstream of receptacle 159 leads to a tube port 148.3 that receives an end of flexible tube 148. The other end of the flexible tube is received within the tube port 148.2 that can be seen in FIG. 17.

Referring to FIGS. 18 and 11B, it can be seen that tube 148 extends from port 148.3 and wraps around the distalmost nose of body 154, and is supported by one or more guiding tube guiding features 148.1. FIG. 11B shows the tube extending between the guiding features 148.1 and flash window 125. Preferably, the portion of tubing proximate to flash window 125 is transparent. The tube then extends aft (i.e., toward the right in FIG. 11B), around the body 154, and past the shoulder wings 165 of sliding disk member 160 (see FIGS. 19B and 19D), and extends finally in a distal direction toward tubing guide 148.4 and into tube port 148.2 of first needle body 144. With this forward-backward-forward again path of tube 148 in the first position, the lower portion of the tube is free to extend aft (i.e., in FIG. 14B to the right) in the second position 112, and thus not impede the retracting motion of needle assembly 140. As best seen in FIG. 14A, it can be seen that tube 148 in the second position extends generally toward one side of the centerline 147, with the end of tube 148 being received within tube holding feature 148.4 of adapter 144.

Apparatus 120 operates in several different modes. FIG. 10 is an exploded view of a storage mode of operation, in which catheter assembly 130 is located at the distal-most end of holder top 124, with full compression of spring 146. Further, in this storage mode, sheath 156 is unpunctured, and maintains the sterility of the internal flowpath of assembly 120.

FIGS. 11A and 11B represent apparatus 120 in a first mode of operation, and with sliding member 160 and needle assembly 140 in a first position 111. Cap 122 has been removed, exposing the sharp tip of cannula 142 and the exterior of flexible lumen 132. The medical practitioner has access to hold the exterior of luer body 134, as well as the ability to hold the exterior of holder top 124 and holder body 126. The medical practitioner places the sharp tip of cannula 140 relative to a vein of a patient, and inserts the cannula 142 and flexible lumen 132 within the vein of the patient.

In the first mode of operation, the medical practitioner can bring a standard collection vessel 110 (not shown) through aperture 129 and into the opened proximal chamber 121 of holder body 126. The proximal end of body 126 includes a generally cylindrical chamber 121. The interior dimensions of the proximal end of holder body 126 are slightly greater than the outer diameter of the collection vessel. Therefore, the collection vessel enters aperture 129, and the face of the collection vessel can be brought into contact with the proximal end of sheath 156.

Preferably, the end of the collection vessel 110 is soft enough such that the medical practitioner can push the collection vessel against sheath 156 and the sharp tip of cannula 152. By continuing to push the collection vessel toward adapter 154, the sharp tip of cannula 152 penetrates the end of collection vessel 110, and enters the interior of the collection vessel. However, the flexible sheath 156 does not enter the collection vessel, and instead is compressed in buckling along cannula 152 and toward adapter body 154.

Once the tip of cannula 152 extends within the empty volume of collection vessel 110, fluid communication is established from the interior of the collection vessel through cannula 152 and adapter body 154, through tube 148, and into the interior flow passage of needle assembly 140. Since needle assembly 140 is exposed to blood within the patient's vein, blood can begin to flow through needle assembly 140 and tube 148, through collection valve assembly 150, and into collection vessel 110.

In order to prevent any hydraulic lockup, the interior of collection vessel 110 can be established at a pressure less than the pressure of the blood within the vein, or a suitable fluid induction device can be used. Still further, any trapped air within needle assembly 140, tube 148, and valve assembly 150 can escape through porous filter 158. However, filter 158 is preferably of a type in which the porosity of the filter is maintained only so long as the filter does not contact blood (such as a POREX® material). Upon contact with the blood, the filter media loses porosity, such that there can be no further leakage of either trapped air or blood through the filter. As blood flows through tube 148, it can be seen by the medical practitioner through a transparent window 125 within holder top 124. The medical practitioner maintains collection vessel 10 within holder body 126 and in fluid communication with the vein of the patient until sufficient blood has been collected. Multiple collection vials maybe used.

After the medical professional has collected sufficient blood, the compression is relieved and the collection vessel 10 is withdrawn. The Adapter 144 assembly still remains in a distal position, and under spring load, until the luer assembly 130 has separated from the holder top 124. The relationship between the luer body 134, Holder top Legs 128 and adapter 144 receiving flats 145 prevent movement.

Once the user advances the catheter luer assembly in a distal direction beyond legs 128, there is nothing to prevent leg 128 from flexing outward. This outward flexing releases Adapter 144 so it can move in a proximal direction, retracting toward the proximal end of holder body 126. Needle assembly 140 can move rearward toward a receiving pocket on the end of disk 160, as seen in FIGS. 12A and 12B. Luer assembly 130 has been removed from its frictional fit over the ears 128 of body 124, thus relieving the normal force applied between the flat 145 of body 144 and the tips of fingers 128. As shown in FIGS. 12A and 12B, with the release of the compression of the fingers into the grooves, needle assembly 140 begins to move from the first position 111 to the second position 112. As shown in FIG. 12B, first needle adapter body 144 is free to move and be guided by the curvature of leg 161. Both disk 160 and needle assembly 140 therefore move toward the proximal end of the body holder.

The beginnings of this movement can be first seen in FIGS. 13A and 13B. Under the influence of the expanding spring 146, needle body 144 has been urged into pocket 127.4 of sliding member 160 and into an intermediate second position 112′. As the proximal-most end of adapter body 144 abuts the internal face of pocket 127.4, the spring force is further exerted on sliding member 160 to move it toward the right. Adapter body 144 and sliding member 160 are shown in an intermediate second position 112′, which is not a steady state location for the assembly as shown in FIG. 13B. In this position 112′, there is still sufficient force being exerted by spring 146 to continue urging apart sliding member 160 and main body 121.1. The full seating of the needle assembly 140 in the receiving pocket 127.4 of disk 160 can be seen in FIG. 13B. Cannula 142 of needle assembly 140 retracts inward toward the interior of main body 121.1. The medical practitioner advances the catheter assembly 130 into the patient's vein, with the result that lumen 132 remains in fluid communication with the patient's vein. However, as needle assembly 140 retracts, the end of the needle assembly retracts past flexible valve 138, which acts as a one-way valve, and thereby closes and prevents any escape of the patient's blood from catheter 130.

FIGS. 14A and 14B show the remaining retraction of needle assembly 140 within holder body 126 to the final, at rest second position 112. As the assembly of the disk and needle retract, tube 148 begins to extend. FIGS. 13A and 13B show the intermediate retraction of needle assembly 140 relative to disk 160. FIGS. 14A and 14B show the completed and full retraction of the sliding disk 160 relative to holder 126. The aft face of disk 160 is biased by spring 146 to sit against a ledge or shoulder surrounding aperture 129 of holder body 126 and locks into place preventing any further movement. Tube 148 is shown in its position of maximum extension from the end of adapter 144 to the end of adapter 154. The sharp tip of cannula 142 is fully contained within holder top 124.

In some embodiments, the relationship between Adapter 144 and disk 160 is generally for guiding disk 160 to its full proximal position. Various embodiments do not include features that pre-stage activation upon insertion of a collection tube 110. The disk 60 statically stays positioned in the holder top 124 by a simple interference fit having a reverse draft. Multiple collection Tubes can be used without activation since activation) retraction of the needle assembly 140 and disk 160) does not occur until the Catheter Luer assembly 130 has separated from the Holder 124.

FIG. 21 show various views of an alternative sliding disk member 260 according to another embodiment of the present invention. Sliding member 260 is substantially the same as sliding member 160 previously described. However, member 260 includes a cylindrical receptacle 227 that extends generally along the length of leg 261. This cylindrically shaped receptacle is open on one side (as best seen in FIGS. 21B and 21E), through which an end of tube 148 can pass. Preferably, the axial length of receptacle 227 is greater than the length of body 144 of needle assembly 140. Further, receptacle 227 preferably extends distally a sufficient amount so that in the first position, the distal end wall of receptacle 227 extends past the proximal end of body 144. This substantially full length receptacle provides additional assurance of proper guiding of assembly 140 in its transition from the first position to the second position, as well as minimizing any possible buckling of spring 148 as it expands going from the first position to the second position.

FIGS. 22-24 pertain to various different apparatus X20 according to still further embodiments of the present invention. These figures show additional aspects of apparatus 320, 420, and 520 that include one or more features to reduce the kinetic energy of the retracting apparatus, including for purposes of reducing any impact or jolt felt by the user as the apparatus changes from the first, extended position to a second, fully retracted position. The use of damping reduces any jolt felt by the user, which aids the user in maintaining proper control of both the inserted catheter and the separated remainder of the assembly which is due for disposal.

In some embodiments of the present invention, there are at least three different pairs of components that have relative motion between the components during the retraction of the first needle assembly X40 and the sliding disk member X60. As nonlimiting examples, there is relative motion between the A adapter X44 and sliding disk member X60 during the initial phase of retraction. There is also sliding motion of disk member X60 relative to holder X24. Additionally, there is relative motion of sliding disk member X60 relative to holder body X26. It is understood that there is relative motion between still further pairs of components, and that the discussion to follow applies to these other pairs as well. It is further understood that the energy dissipation and damping methods shown and described herein can apply to three or more components, and not just to pairs.

FIGS. 22A, 22B, 22D, and 22E show views of portions of an assembly 320 according to another embodiment of the present invention. FIG. 22A shows a damping element 370 that is adapted and configured to dissipate energy, more gradually slow down the moving component, and reduce impact loads from the first retractable needle assembly.

It can be seen that device 370 preferably has a cross sectional shape that is adapted and configured to be partially received within the open, proximal-most end of adapter 344, and generally proximate to tube holder 348.4. In some embodiments, damping element 370 includes an attachment surface 371a that is adapted and configured to be adhered or otherwise attached to the pocket 327.4 of sliding member 360 (as best seen in FIG. 22B). It can be seen that in some embodiments bumper 371 also includes an outer perimeter that contacts the proximal-most face of adapter 344. Further, there is in some embodiments an inner member having a shape that extends within the opened end of adapter 344. Preferably, the distally projecting damper nose is adapted and configured to be the first portion of bumper 371 to contact adapter 344. Preferably this nose is readily deformable. The cross sectional shape of the nose can be of any type (such as conical, truncated conical as shown, rounded, cylindrical, etc.). Still further, the nose or other portions of an impacting bumper according to various embodiments of the present invention contemplate construction that is generally solid across a cross section, and also those that have internal voids that provide additional degrees of deformability.

In some embodiments, portions (or all of) bumper 371 is fabricated from a soft material, such as an elastomeric or other material having a durometer of less than about Shore A40, and in some embodiments having portions with a durometer less than Shore 0040. It is understood that the damping element 370 can be of multiple materials, each with different material characteristics.

FIG. 22D shows the damper 370 placed on the distal side of cover 363. FIG. 22D shows the first needle assembly in the first, fully extended position, with biasing member 346 being placed in a position in which it stores sufficient energy to propel needle assembly 340 in a proximal direction, as indicated by the large arrow. In explained previously herein, after the catheter (not shown) is removed, the coiled spring 346 pushes apart between adapted 344 and holder 324. It is further understood that biasing member 346 can be any type of spring or other elastic member that can store potential energy, and including elastic cords.

FIG. 22E shows the needle assembly 340 in a partially retracted position, with adapter 344 having impacted and compressed damping element 370. By way of this compression of a damping material, some of the kinetic energy of needle assembly 340 is dissipated into the deformation of bumper 371. Further, the reduction in velocity of the retracting needle assembly 340 is reduced over a longer period of time, which reduces the peak g-loading. Because of this dissipation and deceleration, a user having a hand holding the device 320 will feel less impact at this intermediate position.

FIG. 22F shows an apparatus 320-2 according to another embodiment of the present invention. Apparatus 320-2 includes a rub strip 370-2, shown in side view in FIG. 22F and in end view in FIG. 22C. In the various embodiments described herein, a rub strip can be placed on either of the moving components along any sliding pathway in which the relatively sliding components and the rub strip are adapted and configured for sliding, frictional contact.

In comparing FIG. 22F to FIG. 22E, it can be seen that as needle assembly 340-2 is forced in a proximal direction, that the underside of adapter 344-2 will come into sliding contact with the contacting surface 372b-2 of web strip 372. By this sliding contact, some of the kinetic energy of assembly 340-2 is dissipated as friction, thus slowing the assembly prior to the impact of adapter 344-2 onto the distal side of cover 363-2. Further, the velocity of the retracting assembly is reduced from the velocity that the assembly would have had, if the biasing force were unopposed.

In some embodiments, rub strip 372-2 extends in a limited angular sector within pocket 327.4-2, as shown in FIG. 22C. However, yet other embodiments contemplate rub strips having lesser angular extent, or more angular extent. Further, referring to FIG. 22F, in some embodiments the rub strip has an increasing thickness in the proximal direction, and with the proximal-most end of the strip preferably being spaced apart from the distal face of cover 363-2. In so doing, such embodiments exhibit the frictional contact after the compressed spring begins to expand (i.e., where the strip is thinnest), with the frictional loads being relatively low at the beginning of the sliding contact in peaking toward the end of the sliding contact. Preferably, the frictional contact ends prior to contact with sliding member 360-2. In some embodiments, the rub strip 372-2 includes a generally smooth surface, and in still other embodiments a preferably low friction surface, so that the amount of sliding friction can be controlled by the thickness of the strip 372-2 and the geometry of adapter 344-2, rather than being dependent on a rough surface finish.

FIGS. 23A, 23B, and 23C depict various aspects of an apparatus 420 according to another embodiment of the present invention. FIG. 23A shows a holder 424 in which a damping element 470 has been placed. Similar to that described with regards to apparatus 320-2, rub strip 472 has a lower, attachment surface 472a and a top, contacting surface 472b. In some embodiments, the cross sectional shape of the strip (as seen in FIG. 23A) is generally rectangular (i.e., a constant cross sectional thickness). However, rub strips 472 and 372 can be of constant cross sectional thickness, or variable cross sectional thickness. As yet another example, the cross sectional shape (the thickness) could be a pattern of ridges and valleys, such that the motion of the retracting mass exhibits alternating periods of deceleration and acceleration. As a still further variation, and referring to FIG. 22C, it is also appreciated that the angular extent (or width) of the damping element X70 can be variable along the length of the sliding pathway.

FIG. 23B shows the intermediate retracted position of needle assembly 440. Assembly 440 has been received within pocket 427.4, and as a result of this impact, the momentum of assembly 440 carries into sliding cover 460, and spring 446 remains partially compressed and pushing on the sliding member 460 by way of the end of adapter 444. Immediately after the position shown in FIG. 23B, the combination of sliding member 460 and needle assembly 440 both move in a proximal direction and into the interior of holder body 426. In this transition from the intermediate retracted position of FIG. 23B to the fully retracted position of FIG. 23C, there is sliding, frictional contact between the underside of member 460 and damping member 470. In the embodiment shown in FIG. 23C, this frictional contact ends before complete retraction, as evidenced by the gap between the distal end of cover 460 and the proximal end of rub strip 472.

FIGS. 24A, 24B, and 24C show portions of an apparatus 520 according to another embodiment of the present invention. In a device similar to those previously explained, a damping element 570 is placed between a pair of relatively sliding components. Referring to FIG. 24A, it can be seen that a rub strip 572 is attached by surface 572a and placed within a groove 527.2 that comprises a portion of a sliding path by way of a ridge 562 of sliding member 560.

In FIG. 24B, the needle assembly 540 is shown partially retracted, and in contact with sliding member 560. As a result of both spring force and the transfer of momentum, the proximal end of adapter 544 pushes sliding member 560 in a proximal direction, and over the contact surface 572b of rub strip 572. This sliding interaction both decelerates the moving combination of components, and dissipates some of the combined kinetic energy. Referring to FIG. 24C, it can be seen that the proximal end of damping element 570 is preferably displaced distally from the groove 527.3, so as to not interfere with the placement of locking flexible members 564 within the groove.

FIGS. 26-28 present different aspects of an apparatus 620 according to another embodiment of the present invention. As previously stated, it is understood that apparatus 620 can include any of the various features described for any of the apparatus X20 shown herein.

FIG. 26 shows a cutaway of an adapter 654 that provides positioning for a filter 658 and a one-way valve 680 shown in series fluid communication. A filter 658 that provides increased resistance to the flow of blood (such as a POREX © device) has an inlet that is in fluid communication with the inlet 659.2 of a second flowpath 659 defined within body 654. The outlet of filter 658 is preferably in fluid communication with the inlet of a one-way valve 680. The outlet of valve 680 is preferably in fluid communication with the interior 624.3 of body 624.

Although what has been shown a described is a body holding both a filter and a one-way valve, it is understood that the filter and valve can be positioned by any portion of apparatus 620, or by different portions of apparatus 620. Further, although the devices are shown arranged with a particular serial arrangement of the filter and the one-way valve, it is understood a different serial arrangements (such as the outlet of the filter being in fluid communication with the interior of the device 620) is contemplated. Further, it is understood that the exhausting to the material from the filter and valve is preferably to a flash chamber of device 620, such exhausting can take place to other parts of device 620, or to ambient conditions outside of device 620.

FIGS. 27a and 27b show the combination of filter and valve in the opened (flowing) configuration and the closed (restrictive) configuration, respectively. In some embodiments, filter 685 is of the type that will generally permit the flow of gases, but become restrictive to gas flow if that gas includes with it a sufficient flow of a liquid. One example of such a filter is a POREX © Vitek™ Catheter Media. FIG. 27a shows the filter in the prior to use (opened) 685.1 configuration. After a flow of blood reaches the filter, it becomes restrictive to flow as shown in FIG. 27b in the restrictive configuration 658.2.

These two figures also show the operation of the valve 680. Valve 680 is preferably a one-way valve that permits flow in one direction, but restricts flow in the opposite direction. In one embodiment, valve 680 is a miniValve™ umbrella-type valve. The valve is normally closed to flow in a direction from the flash chamber toward the internal flowpaths 652.1 and 659.1, as shown in FIG. 27b. The valve is adapted and configured to open in the opposite direction, i.e. from flowpath 659.1 toward the flash chamber. As shown, valve 680 includes an internal flexible member 681 that opens or closes a plurality of orifices in the periphery of a central member.

FIG. 27a show the initial (prior to usage) configuration of filter 658.1. Initially, filter 658.1 is porous and permits the flow of gas and liquid therethrough. FIG. 28a represents the filter and valve when needle assembly 642 is put in fluid communication with the circulatory system of a person. Since the pressure of the person's blood is higher than the pressure in chamber 624.3 or the pressure at the opened end of second needle 653, blood will enter the first needle 642 and pass through tube 648. Since these passageways also include air, this air is likewise flowing in the needle 642 and tube 648 at the urging of the patient's blood. Further, the pressure of the blood and air are higher than pressure in the flash chamber (or ambient), and therefore the resilient internal valve member 681 is pushed to the opened configuration 680.1 seen in FIG. 27a. Both gas and blood are free to flow through filter 658.1 and valve 680.1 to the flash chamber.

When this flow of blood and gas reaches the filter 658, outward expulsion of gas is permitted until the blood occludes the filter element, as represented in FIG. 27b. Therefore, some blood and gas are free to be vented into the flash chamber, but continued flow of blood is restricted or stopped. Referring to FIG. 28A, blood entering the needle 642 under pressure flows through tube 648 and out through second flowpath 659.2 to the flash chamber via filter 658.1 and valve 680.1. It is noted that in some embodiments, second needle 653 may be enclosed in a sheath 656 (not shown) that restricts flow of blood and gas out through needle 653.

After the medical professional notes the flow of blood into the flash chamber indicating fluid communication with the circulatory system of the patient, a blood sample is withdrawn for laboratory analysis. In some embodiments, this blood sample is taken by an evacuated container 610 that is placed in fluid communication with second needle 653. This communication may be accomplished by pushing the end of the container onto the needle, and puncturing the sheath in those embodiments having a sheath. The system shown in FIG. 28b is shown in a configuration in which the lowest pressure in the flow system is within container 610. Pressure in the patient's circulatory system is higher, such that blood continues to flow inward through the cannular of needle assembly 642. The pressure in the flash chamber 642.3 (or ambient) is also higher than the pressure in evacuated container 610. However, referring to FIG. 27b, this pressure differential across valve 680 is in the direction for which valve 680 in normally closed (i.e., 680.2). Further, the pressure differential across the flexible member 681, which is adapted and configured to close the bottom central inlet of the valve. Therefore, valve 680 is adapted and configured to provide two different function (normally closed, and deflected by pressure differential to close) that result in no gas being pulled into container 610 through second flowpath 659.1. It is understood that yet other embodiments of the present invention contemplate one-way valves that are not normally closed, but instead close under the operation of the pressure differential across the valve. Further, still further embodiment of the present invention that are normally closed, regardless of certain amounts of pressure differential.

Various aspects of different embodiments of the present invention are expressed in paragraphs Z1, Z2, Z3, Z4, Z5, Z6, Z7, Z8, Z9, Z10, and Z11 as follows:

Z1. One aspect of the present invention pertains to an apparatus for collecting blood in a container and connecting to intravenous tubing, comprising a collection cavity adapted and configured to receive therein an end of a readily separable container; a first hollow needle having a first sharp tip, said first needle being adapted and configured for insertion of the first tip into a blood vessel; a second hollow needle having a second sharp tip extending into the collection cavity; and a catheter assembly having a body and a hollow lumen and receiving said first needle within the lumen, the first sharp tip extending from the distal end of the lumen, the catheter body having a proximal end adapted and configured for attachment to the intravenous tubing, said catheter body including a one-way valve; wherein said first needle and said main body are readily separable from said catheter assembly, and said one-way valve prevents flow of blood through the lumen when said first needle is separated from the lumen.

Z2. Another aspect of the present invention pertains to an apparatus for collecting blood in a container and connecting to intravenous tubing, comprising a main body defining an interior adapted and configured with a readily separable container; a first retractable hollow needle having a first sharp tip, said first needle being movable from a first extended position in which the first sharp tip is exterior to said main body to a second retracted position in which the first sharp tip is within the interior; a second hollow needle having a second sharp tip, said second tip not extending outside of said main body; and a catheter assembly having a body and a hollow lumen and receiving said first needle within the lumen, the catheter body having a proximal end adapted and configured for attachment to the intravenous tubing; wherein said first needle and said main body are readily separable from said catheter assembly, said first needle automatically retracting to the second position in response to separating said first needle from said catheter assembly.

Z3. Yet another aspect of the present invention pertains to a method for obtaining a sample of blood in a container from the circulatory system of a biological unit, comprising providing a hand-held device defining an interior including a collection cavity and including first and second hollow needles in fluid communication with each other and a catheter surrounding the first needle; inserting the first needle and the surrounding catheter into the circulatory system; inserting the second needle into the container; establishing fluid communication from the first needle to the container; separating the first needle and the catheter; and automatically retracting the first needle into the interior after said separating.

Z4. Still another aspect of the present invention pertains to an apparatus for collecting blood in a container, comprising a main body including a collection cavity adapted and configured to receive therein an end of a separable container; a first retractable hollow needle slidable within said main body and having a first sharp tip, said first needle having a first extended position for insertion of the first tip into a blood vessel and a second retracted position in which the first tip is protected by said main body; a spring configured to urge said first needle into the second position; a second hollow needle attached to said main body and having a second sharp tip extending into the collection cavity; and a catheter having a hollow lumen and receiving said first needle within the lumen when said first needle is in the first position.

Z5. Still another aspect of the present invention pertain to an apparatus for collecting blood in a container, comprising a main body including a collection cavity adapted and configured to receive therein an end of a separable container; a sliding member guided to slide along a path within the collection cavity from a first position to a second position and including a cover defining an aperture; a first retractable hollow needle coupled to said main body and having a first sharp tip, wherein in the second position the first tip is protected within said main body; a second hollow needle attached to said main body and having a second sharp tip extending through the aperture in the first position into the collection cavity; and a catheter having a hollow lumen and receiving said first needle within the lumen when said first needle is in the first position; wherein said first needle is separated from said lumen in the second position, and said cover protects the user from accidental contact with said second needle in the second position.

Z6. Yet another aspect of the present invention pertains to an apparatus for collecting blood in a container, comprising a main body including a collection cavity adapted and configured to receive therein an end of a separable container; a first retractable hollow needle slidable within said main body and having a first sharp tip, said first needle having a first extended position for insertion of the first tip into a blood vessel and a second retracted position in which the first tip is protected within said main body; a second hollow needle fistedly attached to said main body and having a second sharp tip extending toward the collection cavity; and a catheter having a hollow lumen and receiving said first needle within the lumen when said first needle is in the first position; wherein said first needle is distal to said second needle in the first position, said first needle is separated from said lumen in the second position, and which further comprises a first needle body attached to said first needle, wherein in the second position said first needle body is received within the collection cavity.

Z7. Still another aspect of the present invention pertains to an apparatus for collecting blood in a container, comprising a main body including a collection cavity adapted and configured to receive therein an end of a separable container; a first retractable hollow needle slidable within said main body and having a first sharp tip, said first needle having a first extended position for insertion of the first tip into a blood vessel and a second retracted position in which the first tip is protected within said main body, said first needle being oriented along a first axis; a second hollow needle separate from said first needle and attached to said main body and having a second sharp tip extending into the collection cavity, said second needle being oriented along a second axis that is non-coincident with the first axis; and a catheter having a hollow lumen and receiving said first needle within the lumen when said first needle is in the first position; wherein said first needle is separated from said lumen in the second position.

Z8. Yet another aspect of the present invention pertains to an apparatus for collecting blood in a container, comprising a main body including a collection cavity adapted and configured to receive therein an end of a separable container; a first retractable hollow needle slidable within said main body and having a first sharp tip, said first needle having a first extended position for insertion of the first tip into a blood vessel and a second retracted position in which the first tip is protected within said main body; a second hollow needle separate from said first needle and having a second sharp tip extending into the collection cavity a flexible tube providing fluid communication from said first needle to said second needle in the first position; and a catheter having a hollow lumen and receiving said first needle within the lumen when said first needle is in the first position; wherein said first needle is separated from said lumen in the second position.

Z9. Another aspect of the present invention pertains to an apparatus for collecting fluid from a source, a main body defining an interior including an interior said main body including a sliding pathway, a first retractable needle assembly including a sliding body supporting a first hollow needle with a first sharp tip, said first needle assembly being slidable along the sliding pathway from a first extended position in which the first sharp tip is exterior to said main body to a second retracted position in which the first sharp tip moves in a direction away from the first extended position, means for biasing said first retractable needle assembly from the first position toward the second position, means for resisting the sliding motion of said first needle assembly along the sliding pathway; and a separable assembly having a second body and a hollow lumen and receiving said first needle within the lumen, the first sharp tip extending from the distal end of the lumen, wherein said first needle and said main body are readily separable from said separable assembly, said first needle automatically retracting toward the second position in response to separating said first needle from said catheter assembly.

Z10. Yet another aspect of the present invention pertains to a method for obtaining fluid from a source, comprising: providing a hand-held device defining an interior and including a first hollow needle assembly and a catheter surrounding the first hollow needle assembly; inserting the first needle and the surrounding catheter into the source; establishing fluid communication from the first needle to the source; separating the first needle and the catheter after said establishing; automatically biasing the first needle to move toward the interior by said separating; and resisting the movement of the first needle toward the interior.

Z11. Still another aspect of the present invention pertains to an apparatus for collecting fluid from a source, comprising: a main body including an interior and a sliding pathway; a sliding member guided to slide within the interior and in contact with the sliding pathway from a first position to a second position and including a cover lockable to said main body; a first retractable needle coupled to said main body and having a first tip, wherein in the first position the first tip is extended for insertion into a blood vessel and in the second position the first tip is retracted in a proximal direction relative to the first position; a catheter having a hollow lumen and receiving said first needle within the lumen when said first needle is in the first position; wherein said first needle is separated from said lumen in the second position, and said cover shields the interior in the second position.

Yet other embodiments pertain to any of the previous statements Z1, Z2, Z3, Z4, Z5, Z6, Z7, Z8, Z9, Z10, or Z11 which are combined with one or more of the following other aspects. It is also understood that any of the aforementioned Z paragraphs include listings of individual features that can be combined with individual features of other Z paragraphs.

Which further comprises a transparent member permitting visualization of the flow of blood to said second needle.

Which further comprises a second body coupled to said second needle and providing fluid communication from said first needle to said second needle, said second body including a gas purging valve that permits the escape of gas contained in the fluid flowpath from said first needle to said second needle.

Wherein said catheter body is coupled to said main body by a frictional fit.

Wherein said first needle and said second needle are unitary.

Wherein said first needle and said second needle are non-unitary.

Which further comprises means for automatically retracting said first needle.

Wherein said retraction means includes a spring.

Which further comprises means for preventing automatic retraction of the first needle.

Wherein said preventing means includes a plurality of fingers each received within a corresponding groove, said main body including one of said fingers or said grooves and first needle body including the other of said fingers or said grooves.

Wherein said preventing means includes a frictional fit between said catheter body and said main body.

Wherein after said separating and during said retracting the catheter remains inserted into the circulatory system.

Which further comprises blocking said retracting by said placing.

Wherein said providing includes a cover of the collection cavity, and which further comprises automatically locking the cover to prevent access by the user to the second hollow needle.

Wherein said locking occurs automatically by said separating and by removing the container from the collection cavity.

Which further comprises removing the container from the cavity after said collecting.

Which further comprises collecting blood within the container after said establishing and before said separating.

Wherein said establishing is by puncturing the container with the second needle.

Wherein the device includes a pocket and said retracting is into the pocket.

Wherein said retracting is into the collection cavity.

Wherein said first needle is supported by a needle body having a ridge, said main body includes a recess, and said spring urges the ridge apart from the recess.

Which further comprises a cover for the collection cavity, and said spring is configured to urge said cover to a position preventing access to said second hollow needle.

Wherein said spring is a coil spring.

Wherein said second needle has an axis, the collection cavity has a first length along the axis, said second needle extends into the cavity by a second length along the axis, and the second length is less than the first length.

Which further comprises a flexible sheath surrounding the second sharp tip.

Wherein said sliding member includes a flexible outwardly extending ear, said main body includes a groove adapted and configured to receive the ear therein, said ear and said groove coacting to prevent movement of said sliding member relative to said main body when said first needle is in the first position.

Wherein said sliding member includes a flexible outwardly extending ear, said main body includes a groove adapted and configured to receive the ear therein, said ear and said groove coacting to prevent movement of said sliding member relative to said main body when said first needle is in the second position.

Wherein said sliding member includes an internal pocket, said first needle is received within a first needle body, and said first needle body is coupled to said main body in said first position, and said first needle body is received within the pocket in the second position.

Wherein said sliding member includes a first feature having a cross sectional shape, said main body includes a second feature having a shape complementary to the shape of the first feature, and said first feature and said second feature coact to guide the sliding of said sliding member along the path.

Wherein the cavity has an inner diameter and the cover has an outer diameter substantially the same but less than the inner diameter.

Which further comprises a cover slidable within the collection cavity, said main body has a distalmost end, and said first needle is located between the distalmost end and the cover in the second position

Which further comprises a cover slidable within the collection cavity from a first position in which an aperture of said cover surrounds said first needle, to a second position in which said cover closes the collection cavity and prevents access to said second sharp tip.

Which further comprises a spring adapted and configured to urge apart said main body and said first needle body.

Wherein said first needle body applies a force from said spring to urge said cover to the second position.

Wherein the first axis and the second axis are parallel.

Wherein the first axis and the second axis are displaced from one another.

Wherein the first axis and the second axis are not parallel.

Wherein the second axis extends upward relative to the first axis.

Wherein said tube is adapted and configured to provide fluid communication from said first needle to said second needle in the second position.

Wherein said main body includes a window, and said flexible tube can be viewed through the window.

Wherein in the first position said first needle is generally distal to said second needle, and in the second position said first needle is generally adjacent to said second needle.

Wherein said first needle is received within a first needle body, wherein said sliding member includes a receptacle for receiving said hollow needle body, said receptacle at least partially enclosing said hollow needle body in the first position.

While the inventions have been illustrated and described in detail in the drawings and foregoing description, the same is to be considered as illustrative and not restrictive in character, it being understood that only certain embodiments have been shown and described and that all changes and modifications that come within the spirit of the invention are desired to be protected.

Wherein said biasing means is a spring.

Wherein said biasing means is an elastic cord.

Wherein said sliding pathway is adapted and configured to slidingly contact said first needle assembly during movement from the first position to the second position.

Wherein said resisting means includes guiding said first needle assembly to contact the sliding pathway.

Wherein the sliding pathway includes a coating adapted and configured to reduce the sliding friction coefficient of the sliding pathway.

Wherein the sliding pathway includes a rub strip adapted and configured for contact with said first needle assembly.

Wherein the first needle assembly includes a coating adapted and configured to reduce the sliding friction coefficient of the sliding body.

Wherein said resisting is by sliding contact between the first hollow needle assembly and another surface of the hand-held device.

Wherein said device includes a slidable cover, and said resisting is by sliding contact between the cover and another surface of the hand-held device.

Wherein said device includes a slidable cover, and said resisting is by impacting the cover and a deformable surface of the hand-held device.

Wherein said resisting includes impacting the first hollow needle assembly and a surface of the hand-held device.

Wherein the surface includes a deformable material.

Wherein the first hollow needle assembly includes a deformable material.

Wherein the hand-held device includes a deformable surface, and said resisting is by deforming the deformable surface by the impact.

Wherein said automatically biasing imparts kinetic energy into the first needle, and said resisting frictionally dissipates some of the kinetic energy.

Which further comprises an elastic member adapted and configured to store sufficient energy to force said sliding member from the first position to the second position, and the contact between the sliding pathway and said sliding member frictionally dissipates some of the kinetic energy of said sliding member but prevent the cover from locking to said main body.

Claims

1. An apparatus for intravenous withdrawal of blood, comprising: a main body defining an interior;a catheter assembly having a body and a hollow lumen having a distal open end;a first hollow needle having a first sharp tip, said first needle being readily movable relative to said catheter assembly from a first extended position in which the first sharp tip extends from the distal open end of said lumen to a second retracted position in which the first sharp tip does not extend from the distal open end of said lumen;a second hollow needle having a second sharp tip extending in a direction opposite to the direction of the first hollow needle, said first hollow needle and said second hollow needle having a fluid flowpath therebetween;means for purging the fluid flowpath to the interior of said body; andmeans for restricting said purging means.

2. The apparatus of claim 1 wherein said restricting means is operative to restrict flow in the presence of blood.

3. The apparatus of claim 1 wherein said restricting means permits flow into the fluid flowpath.

4. The apparatus of claim 1 which further comprises means for biasing apart said first hollow needle and said catheter assembly.

5. The apparatus of claim 4 wherein said biasing mean is a spring.

6. The apparatus of claim 1 wherein said purging means permits flow in one direction and restricts flow in the opposite direction.

7. An apparatus for collecting blood, comprising: a main body defining an interior;a first retractable hollow needle having a first sharp tip extending distally, said first needle being movable from a first extended position in which the first sharp tip is exterior to said main body for insertion into a blood vessel to a second retracted position in which the first sharp tip is within the interior;a second hollow needle attached to said main body and having a second sharp tip extending proximally;a catheter assembly having a body and a hollow lumen and receiving said first needle within the lumen;a tube adapted and configured to provide a fluid flowpath from said first needle to said second needle; anda first one-way valve that discourages the intake of gas into the fluid flowpath and permits the flow of gas out of the fluid flowpath;wherein said first needle is readily separable from said catheter assembly.

8. The apparatus of claim 1 which further comprises a second one-way valve that discourages the escape of gas from the fluid flowpath.

9. The apparatus of claim 8 wherein said first one-way valve and said second one-way valve are arranged in series.

10. The apparatus of claim 8 wherein said second one-way valve has an inner flowpath that includes a porous element, the porous element being adapted and configured to become restrictive in the presence of blood.

11. A method for withdrawing blood from a biological unit, comprising: flowing blood in the lumen of a hollow needle to the inlet of a first branching flowpath and to the inlet of a second branching flowpath;permitting the flow of gas out of the outlet of the second branching flowpath before said flowing blood to the inlet of the second branching flowpath;restricting the flow of gas out of the outlet of the second branching flowpath after said flowing blood to the inlet of the second branching flowpath;applying suction to the outlet of the first branching flowpath; andclosing the second branching flowpath by said applying suction.

12. The method of claim 11 which further comprises restricting the flow of blood through the second branching flowpath after said flowing blood.

13. The method of claim 11 which further comprises permitting the flow of blood out of the outlet of the second branching flowpath before said restricting the flow of gas.

14. The method of claim 11 which further comprises permitting flow of blood in the first branching flowpath.

15. The method of claim 11 wherein said applying suction is by placing an evacuated container in fluid communication with the first branching flowpath.

16. The method of claim 11 wherein said applying suction is by manual operation of a syringe in fluid communication with the first branching flowpath.

17. The method of claim 11 wherein the first branching flowpath is directed to a container for collecting the withdrawn blood.