The present invention relates to devices, assemblies and systems adapted for capturing information in respect of rotational movement. In a specific aspect the invention addresses issues relating to electronic dose data capturing in and for a drug delivery device.
In the disclosure of the present invention reference is mostly made to the treatment of diabetes by delivery of insulin using a drug delivery device, however, this is only an exemplary use of the present invention.
Drug delivery devices have greatly improved the lives of patients who must self-administer drugs and biological agents. Drug delivery devices may take many forms, including simple disposable devices that are little more than an ampoule with an injection means or they may be durable devices adapted to be used with pre-filled cartridges. Regardless of their form and type, they have proven to be great aids in assisting patients to self-administer injectable drugs and biological agents. They also greatly assist care givers in administering injectable medicines to those incapable of performing self-injections.
Performing the necessary insulin injection at the right time and in the right size is essential for managing diabetes, i.e. compliance with the specified insulin regimen is important. In order to make it possible for medical personnel to determine the effectiveness of a prescribed dosage pattern, diabetes patients are encouraged to keep a log of the size and time of each injection. However, such logs are normally kept in handwritten notebooks, from the logged information may not be easily uploaded to a computer for data processing. Furthermore, as only events, which are noted by the patient, are logged, the note book system requires that the patient remembers to log each injection, if the logged information is to have any value in the treatment of the patient's disease. A missing or erroneous record in the log results in a misleading picture of the injection history and thus a misleading basis for the medical personnel's decision making with respect to future medication. Accordingly, it may be desirable to automate the logging of ejection information from medication delivery systems.
Correspondingly, a number of drug delivery devices with a dose monitoring/acquisition feature has been provided or suggested, see e.g. in US 2009/0318865, WO 2010/052275 and U.S. Pat. No. 7,008,399. However, most devices of today are without it.
When providing a drug delivery with a monitoring feature, a rotary sensor may be incorporated to detect relative movement between components of the drug delivery mechanism, the movement being indicative of a set and/or expelled dose of drug. A traditional rotary sensor is discloses in e.g. WO 96/19872 comprising a code disc with code segments and a reference track arranged in two ring-shaped structures as well as a contact structure for each ring structure.
Having regard to the above, it is an object of the present invention to provide a drug delivery device as well as components and assemblies therefore which in a safe, user-friendly, cost-effective and reliable way allows detection and storage of dose data related to use of a drug delivery device. It is a further object to provide such components and assemblies which could be used also in other applications having the same types of input.
In the disclosure of the present invention, embodiments and aspects will be described which will address one or more of the above objects or which will address objects apparent from the below disclosure as well as from the description of exemplary embodiments.
Thus, in a first aspect of the invention a sensor assembly is provided comprising a first rotary sensor part and a second rotary sensor part. The first rotary sensor part comprises a surface having a circumferentially arranged reference track, and a plurality of individual electrically conducting code segments arranged in a pattern. Each code segment is arranged in the reference track but electrically isolated therefrom, whereby a plurality of electrically conducting reference segments are formed between the code segments. The second rotary sensor part is arranged rotationally relative to the first part and comprises a plurality of contact structures, each contact structure being arranged to be in contact with either a code segment or a reference segment depending on the rotational position between the first and second rotary sensor part. The contact structures are configured to engage and connect to different sensor segments as the first and second rotary sensor part rotate relative to each, the created connections being indicative of a rotational position between the first and second rotary sensor part. For a given rotational position, at least one contact structure engages a code segment and at least one contact structure engages a reference segment.
The term “given rotational position” is meant to cover normal operational states in which a given switch contact is positioned in contact with a single sensor or reference segment, i.e. outside the gaps formed between two neighbouring sensor segments.
By such an arrangement one or more of the following can be achieved: Minimizing physical volume of a positional sensor by having both reference (ground) connections and code information on the same track, and by using the same contact structures for both code and reference connection. Simplification of sensor segments part by removal of dedicated reference connection and using contact structures dynamically for both code and reference connections. By the above features a sensor design is provided which in itself allows a smaller and simpler sensor to be manufactured in a cost-effective way, but also provides a higher degree of freedom of design when incorporating the sensor system in a given mechanical construction such as a drug delivery device.
The second rotary sensor part may be in the form of a metallic disc member comprising a plurality of integrally formed flexible arms forming the contact structures.
The reference segments may be electrically connected to each other to thereby form a single conductive structure, this allowing a simple design with only a single electric connection between the interconnected reference segments on the first rotary sensor part and the associated electronic circuitry of the sensor assembly. For example, the code segments may be arranged in the reference track as “islands” surrounded by conducting portions of the reference track on both side, or alternatively with conducting portions on only one side. As a further alternative the reference segments may be connected with conductors arranged on the opposed surface.
The reference segments and the code segments may be formed on the first rotary sensor part surface by a plating process, especially, the reference segments, the electrical connections there between, and the code segments may be formed on the first rotary sensor part surface by a plating process.
The first rotary sensor part may further be provided with one or more circumferentially arranged switch segments, the second rotary sensor part comprising one or more contact structures providing an axial switch contact having a connected position in which the switch contact is in contact with a sensor switch segment and a dis-connected position in which the switch contact is not in contact with a sensor switch segment.
The sensor assembly may further comprise electronic circuitry adapted to determine a rotational position between the first and second rotary sensor part based on a given pattern of created connections.
In an exemplary application the rotary sensor assembly can be incorporated cost-effectively and reliably in a drug delivery device comprising a rotational member which rotates corresponding to a set and/or expelled dose.
Correspondingly, in an exemplary embodiment a drug delivery device is provided comprising a sensor assembly as described above, the drug delivery device further comprising a housing, a drug-filled cartridge or means for receiving a drug-filled cartridge, and drug expelling means, the cartridge comprising an axially displaceable piston and a distal outlet portion. The drug expelling means comprises dose setting means allowing a user to set a dose of drug to be expelled, an axially displaceable piston rod adapted to move the piston of a cartridge in a distal direction to thereby expel drug from the cartridge, a rotational member adapted to rotate corresponding to a set and/or expelled dose, and an axially moveable actuation member adapted to actuate the drug expelling means to thereby expel the set dose of drug. In such an arrangement the first and second rotary sensor parts rotate relative to each other during setting and/or expelling of a dose of drug.
The first portion of the sensor assembly may be mounted to and rotate with the rotational member, the first portion comprising electronic circuitry adapted to estimate an amount of expelled drug based on detection of rotational movement between the first and second portions corresponding to a set and/or expelled dose. The rotational member may be adapted to move axially between an initial and an actuated position, the first portion of the sensor assembly being mounted to move axially with the rotational member. Also the second portion may be mounted to move axially with the rotational member. For such a design the inherent movements of the rotational member can be detected simple and effectively by the sensor assembly when provided with axial switch means.
The electronic circuitry may be provided with logging means adapted to create a log for dose amounts of drug expelled from a cartridge by the drug expelling means, the dose amounts being calculated based on relative rotation between the first and second rotary sensor parts during setting and/or expelling of a dose of drug. The electronic circuitry may be provided with transmitter means adapted to transmit stored data to an external receiver. Alternatively or in addition, the first portion may comprise a display which may be controlled to be turned off during rotation of the first portion.
In a specific embodiment of the invention a drug delivery device is provided comprising a housing, a drug-filled cartridge or means for receiving a drug-filled cartridge, and drug expelling means, the cartridge comprising an axially displaceable piston and a distal outlet portion. The drug expelling means comprises dose setting means allowing a user to set a dose of drug to be expelled, an axially displaceable piston rod adapted to move the piston of a cartridge in a distal direction to thereby expel drug from the cartridge, a rotational member adapted to rotate corresponding to a set and/or expelled dose, and an axially moveable actuation member adapted to actuate the drug expelling means to thereby expel the set dose of drug. The drug delivery device further comprises sensor means adapted to detect a set and/or an expelled dose, comprising (i) a first portion comprising a first rotary sensor part, the first rotary sensor part comprising a surface with a plurality of sensor and reference segments forming a combined code and reference track as described above, and (ii) a second portion comprising a second rotary sensor part arranged rotationally relative to the first portion, the second rotary sensor part comprising a plurality of combined code and reference contact structures as described above. One of the contact structures may comprise an axial switch contact having a connected position in which the switch contact is in contact with a sensor area and a dis-connected position in which the switch contact is not in contact with a sensor area. The first and second rotary sensor parts rotate relative to each other during setting and/or expelling of a dose of drug, and the axial switch is actuated between its two positions when the actuation member is moved axially.
The electronic circuitry may be adapted to determine a rotational position between the first and second portions based on a given pattern of created connections, the electronic circuitry comprising logging means adapted to create a log for dose amounts of drug expelled from a cartridge by the drug expelling means, wherein the dose amounts are calculated based on relative rotation between the first and second rotary sensor parts during setting and/or expelling of a dose of drug. The drug delivery device may comprise additional features as described above.
In a second aspect of the invention a sensor assembly, e.g. a rotary encoder disc assembly, is provided comprising an electrical connector structure comprising at least one terminal, a non-conducting moulded matrix member, and at least one conducting structure having a contact surface. A portion of the electrical connector structure comprising at least one terminal is in-moulded in the matrix member, at least one conducting structure is in-moulded in the matrix member with at least a portion of the contact surface being free, and at least one in-moulded conducting structure is connected to an in-moulded terminal.
A sensor member such as a rotary encoder disc comprises a disc with a code pattern as well as a connector structure allowing the conductive areas of the code pattern to be connected to a PCB, e.g. using a traditional male-female connector. By in-moulding the terminals of an electrical connector structure, e.g. a flex-connector, in a non-conductive disc matrix and creating the conductive code areas by in-moulding, a compact and reliable sensor assembly is provided. In a most simple embodiment a single conductive structure providing a single contact surface is in-moulded in direct contact with a single terminal.
The at least one conducting structure may be formed from a conducting polymer, the matrix member and the at least one conducting structure being formed by two-shot moulding.
For a more complex sensor assembly it may further comprise at least one conducting connector structure connecting a conducting structure and a terminal, wherein at least one conducting connector structure is in-moulded in the matrix member, e.g. during the two-shot moulding.
In an exemplary embodiment the matrix member comprises a first surface with at least one cavity with an in-moulded conducting structure, and a second opposed surface with at least one cavity with an in-moulded conducting connector structure, the conducting structure and the conducting connector structure being connected to each other through an opening formed in the matrix member, the conducting connector structure being connected to a terminal.
In a third aspect of the invention a rotary sensor member adapted to rotate corresponding to an axis of rotation is provided, comprising at least two surfaces, wherein the first surface comprises a plurality of individual electrically conducting encoder sensor segments arranged in a circumferential pattern, and the second surface comprises a further circumferential track in the form of a ground track or a second code track having a second plurality of individual electrically conducting encoder sensor segments arranged in a second circumferential pattern.
By arranging the two circumferential structures on two different surfaces of a rotary sensor member, e.g. opposed sides of a disc, the desired functionality can be achieved with a sensor member having a small diameter. Further, by separating the two circumferential structures on two surfaces the risk of short circuit is reduced.
In an exemplary embodiment the rotary sensor member may comprise at least two surfaces arranged axially offset and perpendicularly relative to the axis of rotation, e.g. in the form of the two opposed surfaces on a disc member. The surfaces will typically be generally planar.
The rotary sensor member may comprise at least one generally cylindrical surface, each generally cylindrical surface, when more than one generally cylindrical surface is provided, being arranged radially offset relative to the axis of rotation.
The rotary sensor member may comprise at least three surfaces and at least one further circumferential track in the form of a (further) ground track or a further code track.
In an exemplary embodiment a sensor assembly is provided comprising a rotary sensor member as described above, further comprising a plurality of switch contact structures, each switch contact structure being arranged for sliding rotational engagement with a circumferential pattern or a circumferential track.
As used herein, the term “drug” is meant to encompass any flowable medicine formulation capable of being passed through a delivery means such as a cannula or hollow needle in a controlled manner, such as a liquid, solution, gel or fine suspension, and containing one or more drug agents. The drug may be a single drug compound or a premixed or co-formulated multiple drug compounds drug agent from a single reservoir. Representative drugs include pharmaceuticals such as peptides (e.g. insulins, insulin containing drugs, GLP-1 containing drugs as well as derivatives thereof), proteins, and hormones, biologically derived or active agents, hormonal and gene based agents, nutritional formulas and other substances in both solid (dispensed) or liquid form. In the description of the exemplary embodiments reference will be made to the use of insulin and GLP-1 containing drugs, this including analogues thereof as well as combinations with one or more other drugs.
In the following the invention will be further described with reference to the drawings, wherein
In the figures like structures are mainly identified by like reference numerals.
When in the following terms such as “upper” and “lower”, “right” and “left”, “horizontal” and “vertical” or similar relative expressions are used, these only refer to the appended figures and not necessarily to an actual situation of use. The shown figures are schematic representations for which reason the configuration of the different structures as well as their relative dimensions are intended to serve illustrative purposes only. When the term member or element is used for a given component it generally indicates that in the described embodiment the component is a unitary component, however, the same member or element may alternatively comprise a number of sub-components just as two or more of the described components could be provided as unitary components, e.g. manufactured as a single injection moulded part. When it is defined that members are mounted axially free to each other it generally indicates that they can be moved relative to each other, typically between defined stop positions whereas when it is defined that members are mounted rotationally free to each other it generally indicates that they can be rotated relative to each other either freely or between defined stop positions. The terms “assembly” and “subassembly” do not imply that the described components necessary can be assembled to provide a unitary or functional assembly or subassembly during a given assembly procedure but is merely used to describe components grouped together as being functionally more closely related.
Referring to
More specifically, the pen device comprises a cap part (not shown) and a main part having a proximal body or drive assembly portion 120 with a housing 121 in which a drug expelling mechanism is arranged or integrated, and a distal cartridge holder portion in which a drug-filled transparent cartridge 180 with a distal needle-penetrable septum can be arranged and retained in place by a cartridge holder 110 attached to the proximal portion, the cartridge holder having openings allowing a portion of the cartridge to be inspected. The cartridge may for example contain an insulin, GLP-1 or growth hormone formulation. The device is designed to be loaded by the user with a new cartridge through a distal receiving opening in the cartridge holder, the cartridge being provided with a piston driven by a piston rod 128 forming part of the expelling mechanism. A proximal-most rotatable dose ring member 125 serves to manually set a desired dose of drug shown in display window 126 and which can then be expelled when the release button 127 is actuated. Depending on the type of expelling mechanism embodied in the drug delivery device, the expelling mechanism may comprise a spring which is strained during dose setting and then released to drive the piston rod when the release button is actuated. Alternatively the expelling mechanism may be fully manual in which case the dose ring member and the release button moves proximally during dose setting corresponding to the set dose size, and then moved distally by the user to expel the set dose. The cartridge is provided with distal coupling means in the form of a needle hub mount 182 having, in the shown example, an external thread 185 adapted to engage an inner thread of a corresponding hub of a needle assembly. In alternative embodiments the thread may be combined with or replaced by other connection means, e.g. a bayonet coupling.
The cartridge holder comprises a distal opening adapted to receive a cartridge. More specifically, the cartridge holder comprises an outer rotatable tube member 170 operated by the user to control movement of gripping means to thereby open and close gripping shoulders 145 configured to grip and hold a cartridge.
As appears,
With reference to
The different components of the logging module 300 are shown in
The second rotary sensor part 330 shown in
In this way a given pair of contact arms provides a combined contact structure adapted to create electric contact between two contact segments. In the shown embodiment the two inner ground contact arms 331 are provided to be in contact with the single ground contact area 321 of the inner concentric ring, the three position contacts arms 332 are provided to be in contact with the four position contact segments 322 of the intermediate concentric ring, and the two outer switch contact arms 333 are provided to be in contact with the three switch contact segments 323 of the outer concentric ring, the outer switch contact arms carrying a laterally extending projection 334. Indeed, for the intermediate and outer contact arms the rotational position between the two sensor parts will determine which contact segment is engaged with a given contact arm.
In the shown embodiment the gaps between two neighbouring outer contact segments are dimensioned such that the dome-formed contact point will be in contact with both segments as it moves from one segment to the next, this being explained in greater detail below. The second rotary sensor part further comprises a gripping part 336 adapted to engage the projection 337 on the rotary sensor holder 339 to prevent rotational movement there between.
In the shown embodiment the intermediate arms and contact segments provide the rotary sensor contacts whereas the outer arms and contact segments provide an axial switch as will be described in greater detail below.
The button 240 with the window 241 attached is mounted on the module housing in gripping engagement with the circumferential groove 315, this allowing the button to rotate relative to the module housing. The axially compressed button assembly spring 242 is arranged in the circumferential gap between the module housing and the dial ring member and held in place between a distally facing ring portion of the button ring and the proximally facing portion of the coupling flange. In this way the spring provides an axial force biasing the module proximally into non-rotational engagement with the dial ring member 230 via the coupling flange, however, when a distally directed force is applied to the module via the button the module can be moved distally and thereby out of the rotational coupling with the dial ring member, this allowing the logging module main housing to rotate relative to the dial ring member.
As indicated above, the shown rotary sensor comprises an axial switch, this switch serving to detect an axial position of the logging module relative to (here) the housing member 220. More specifically,
Returning to the first and second rotary sensor parts of
In respect of the above-described axial switch, using only one switch there would be a single point of failure when the information is to be detected by electrical means. Correspondingly, as shown in
More specifically, as shown in
In case the arms are not pressed down, the values for the three segments are 1,1,1.
If one of the switch contact segments or contact arms is faulty, the code pattern will be different from the above pattern. For example, if MS1 is faulty with the value “1” when the arms are pressed down then the first code would be 1,0,1. This fault is detectable since only one of the segments has the value “0” (at least two “0” is expected in a healthy system), this allowing a single contact failure to be detected. Theoretically, if one functioning contact arm was bridging the gap between two neighbouring sensor areas and the other contact arm was faulty, then this would represent a non-error condition with two “0” values. However, if error detection is performed during rotation this special condition could be detected and disregarded. If MS1 is faulty with the value “0” when the arms are not pressed down then this fault is detectable since the values for the three segments should be 1,1,1 when the arms are not pressed down.
Although not implemented in the described embodiment, the outer contacts could also be used to provide additional rotational position information to the system.
Returning to the first and second rotary sensor parts of
In an alternative embodiment shown schematically in
In the shown embodiment the code segments, the ground segments and the individual combined code and ground contact arms are arranged such that for a given rotational position at least one of the arms will be in contact with a ground segment, the remaining arms being in contact with a code segment to provide positional information. As appears, by this arrangement it is possible to maintain the same functionality as with two separate tracks and dedicated arms for each track, the design allowing a more compact and simpler sensor to be manufactured.
Addressing the issue of providing a rotary sensor which is both compact and reliable, a further embodiment of a rotary sensor component as well as a method of manufacture using two-shot moulding will be described with reference to
As appears, for illustrative purposes the sensor component 560 of
Addressing the issue of providing a rotary sensor which is both compact and reliable, a yet further embodiment of a rotary sensor component will be described with reference to
The three planar and two cylindrical surfaces provide a total of five surfaces which each may serve as a carrier for one or more circumferential sensor tracks. In the shown embodiment a first circumferential code track with a plurality of discrete contact areas 652 is formed on the first planar surface 661, a second circumferential code track with a plurality of discrete contact areas 656 is formed on the outer second cylindrical surface 665, a third circumferential code track with a plurality of discrete contact areas 657 is formed on the first cylindrical edge surface 663, a fourth circumferential code track with a plurality of discrete contact areas 659 is formed on the inner third cylindrical surface 666 and a circumferential ground track 658 is formed on the second planar surface 662. A further track may be formed on the not seen lower second planar surface.
In respect of the embodiment of
By providing a rotary sensor member with a plurality of planar and cylindrical surfaces a larger number of tracks can be formed for a given diameter size of the sensor member.
The parts of the subassembly 200, apart from module 300, as shown in
Although not part of the present invention, in the following a short description of a drug expelling mechanism into which the shown inner tube member 210 could be integrated will be described. When setting a dose to be expelled the user rotates the dial ring member 230 and thereby the inner tube member 210 to a given rotational position representing a desired dose, this straining a torsional spring member arranged around the tube member and attached at its proximal end to a housing proximal portion and at its distal end to the tube member distal portion. A ratchet coupling arranged at the distal end of the inner tube member serves to hold the now rotationally biased tube member in the set position. A scale drum is coupled to and rotates with the tube member, the scale drum having a threaded connection with the housing (e.g. threads 226 in
As appears, in the described exemplary mechanism the inner tube member 210 (to which the main portion of the logging module 300 is rigidly mounted) rotates relative to the housing 220 during both setting and expelling of a given dose. As the second rotary sensor part 330 is rotationally locked to the housing, also the two rotary sensor parts 320, 330 rotate relative to each other during both setting and expelling of a given dose. As this is merely an exemplary mechanism, other mechanisms can be envisaged in which a given member rotates only during setting or expelling.
This said, in the shown embodiment the logging module is adapted to detect rotation in both directions corresponding to a set dose and an expelled dose. In the shown embodiment the logging module is further provided with an axial switch allowing the module to detect whether the mechanism is in the setting or expelling mode, however, this is an optional feature. In the shown embodiment the code pattern has a step “resolution” of 15 degrees of rotations which for a given drug formulation and delivery device combination may correspond to 1 unit (IU) of insulin. Indeed, for a drug formulation having the double concentration a 7.5 degree rotary resolution would be necessary to register dose steps corresponding to 1 IU of insulin. The rotary sensor comprising the rotary contacts and the associated electronic circuitry could be designed to detect the amount of rotation using a number of designs, e.g. each 15 degrees increment may be counted, or a given position may be detected absolutely within sectors of e.g. 120 or 360 degrees, a counter registering the number of completed sectors. Such a counter could be implemented using the switch arms and outer contact areas described with reference to
In an exemplary embodiment the rotary sensor is designed to count the number of steps during setting and to count down the number of steps during expelling, with the expelling steps being registered in the log as the dose being expelled. By counting in both directions proper registering and functioning of the logging module can be assured to a high degree. As a given dose of drug, especially if large, may be divided and injected with a given pause, the logging module may be programmed to log two dose amounts expelled within a given time window, e.g. 15 minutes, as one dose.
The logging module may be configured to store and show data in different ways. To many users the time since last dose and the size of that dose are the most important values. To other users and/or a medical practitioner an overview of the entire log for a given period, e.g. a week or a month, may be of importance. To allow such an overview the logging module may be provided with output means allowing the dose log to be transferred, e.g. by NFC transfer, to an external display device, e.g. a smartphone or computer for better graphic overview, see below.
To ensure that the full dose is expelled the logging module may be set up to display the last expelled dose only when the expelling mechanism has been returned to zero. Otherwise a given “half” dose will be stored in the log but not displayed. For example, if a dose of 40 IU is dialed and 20 IU are expelled immediately thereafter the display will not show data for that delivery. To have the dose shown in the display the user may expel the remaining dose and the combined dose of 40 IU together with a time stamp will be shown in the display. Alternatively the user may dial the expelling mechanism back to zero and the display will show 20 IU, or the user may dial the expelling mechanism back to 10 IU and expel the 10 IU and the display will show 30 IU. Indeed, for the expelled amounts to be combined the two (or more) doses will have to be expelled within the above-described time window, e.g. 15 minutes. Otherwise only the last portion of the dose will display, the first portion being stored merely as an entry in the log.
The display can be configured to show data in different formats. For example, the display 711 of
To save energy the display will turn off after a pre-determined amount of time, e.g. 30 seconds. To turn on the display again the user may e.g. press the button thereby using the axial switch to turn on the display, or the display may be turned on when the dose dial is turned away from and then back to zero.
A user may desire to check the dose log directly on the module display. Toggling through the dose log could also be controlled by the axial switch, e.g. two fast pushes on the button 712 will bring the module into log display mode, each consecutive push on the button recalling the next log entry. The module may leave the log display mode automatically after a given amount of time, or the user may bring the module into normal display mode by e.g. dialling back and forth as described above. As an alternative, the electronic module may be provided with other types of input means, e.g. a motion sensor which would allow a user to turn on the display by shaking or tapping, or a touch sensor integrated in the display as is well known from e.g. smartphones which would allow a user to turn on the display by swiping a finger across the display.
In order to communicate with the logging module the smartphone has been provided with specific “insulin diary” software. When the software is activated to initiate data transfer the smartphone NFC transmitter will transmit specific code which will wake up any nearby logging module which will then retransmit a unique code identifying the specific module. If a specific code is received for the first time the user is asked to confirm pairing and is asked to select from a list the given drug that should be associated with the given logging module, e.g. “Mix 30” as shown. In this way the smartphone can create an insulin diary covering more than one drug. In the described simple “manual” set-up the user has to ensure that a correct cartridge, e.g. with Mix 30 insulin, is loaded in a drug delivery pen which has been associated with that type of drug. Indeed, other set-ups can be envisaged, e.g. a given pen may be (mechanically) coded to only accept a given type of cartridge with the designated type of drug, or the pen and logging module may be provided with the ability to identify different types of cartridges and thus types of drug.
In the shown embodiment log data from a logging module associated with a Mix 30 insulin has been transferred. In the exemplary user interface the user can toggle back and forth between different day views, each day view showing the different amounts of drug delivered together with a real time value. In
In the above description of exemplary embodiments, the different structures and means providing the described functionality for the different components have been described to a degree to which the concept of the present invention will be apparent to the skilled reader. The detailed construction and specification for the different components are considered the object of a normal design procedure performed by the skilled person along the lines set out in the present specification.
Number | Date | Country | Kind |
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13193882 | Nov 2013 | EP | regional |
This application is a 35 U.S.C. § 371 National Stage application of International Application PCT/EP2014/075179 (published as WO2015/075134), filed Nov. 20, 2014, which claims priority to European Patent Application 13193882.1, filed Nov. 21, 2013; this application claims priority under 35 U.S.C. § 119 to U.S. Provisional Application 61/907,488; filed Nov. 22, 2013.
Filing Document | Filing Date | Country | Kind |
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PCT/EP2014/075179 | 11/20/2014 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
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WO2015/075134 | 5/28/2015 | WO | A |
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