The present application is directed to systems, methods and devices used in medical related testing and/or diagnostics and more particularly to systems, methods and devices to collect liquid and/or tissue samples to be used for, for example, testing or diagnosing patients or the like for a particular disease, illness, condition or predisposition.
Liquid and/or tissue specimens or samples may be extracted from a patient or the like through the mouth, nose, or other parts of the body. Collecting samples from the nose can be particularly challenging due to the varying depth necessary to reach an area to obtain a viable and accurate sample.
Once at the optimal area, sufficient liquid and/or tissue needs to be collected. Inadequate collection can cause inaccurate tests or diagnoses. Inadequate collection may also be a result of not collecting a sufficient amount of the desired sample within the allotted collection time.
Accelerating or increasing the collection of the sample thus may further ensure that the quantity and/or viability of the sample is optimally collected while also simultaneously reducing patient discomfort and operational difficulties or challenges. Retaining the sample to be contained or transferred and releasing a sufficient amount of the collected sample to be tested can also be a challenge.
Disclosed herein are a variety of different collection swabs. The collection swabs are made of at least a handle portion that is used to maneuver the collection swab within a desired location of a patient and a distal or tip portion that is designed to collect specimen, tissue, or fluids located at the desired location of the patient such as a nasal cavity. The distal or tip portion is also designed to retain the specimen, tissue, or fluids collected from the patient after the collection swab is removed from the desired location.
Other embodiments of the collection swabs further include a sleeve or cage that is connected to and encompasses the distal or tip portion of the collection swab. The sleeve or cage provides further design space affecting how the collection swab collects and retains the specimen, tissue, or fluids being obtained from the patient. In some cases, the sleeve or cage can be designed to collect the specimen, tissue, or fluids and transfer the collected specimen, tissue, or fluids into an interior space of the sleeve or cage. This allows the enclosed distal or tip portion to capture and retain the specimen, tissue, or fluids from the desired space without having the distal or tip portion interact with the desired space directly. Alternatively, the sleeve or cage can also collect and retain any specimen, tissue, or fluid along with the distal or tip portion of the collection swab.
In accordance with various embodiments, a collection system is provided. In various embodiments, the collection system comprises a collection swab and a collection container. In various embodiments, the collection swab is a nasopharyngeal swab and the collection container is configured to receive a distal portion of the collection swab for the depositing of a collected sample, specimen, or the like. In various embodiments, the collection swab comprises a shaft and a cover or sleeve. In various embodiments, the collection swab comprises a shaft and no cover or sleeve. In various embodiments, the collection swab comprises a shaft with a distal end or portion with or without a sleeve. The sleeve is configured to retrieve a test sample from a patient's nasopharynx or other anatomical locations. Nasopharyngeal swabs are required to obtain patient nasal secretions to test for the presence of respiratory viruses such as COVID-19, and in accordance with various embodiments, the collection swab comprising the shaft and/or the sleeve provides such a nasopharyngeal swab.
In accordance with various embodiments and as shown, for example in the figures of the present application, a collection system and/or various portions and embodiments thereof are provided. With respect to
With respect to the embodiment illustrated in
In various embodiments, the distal or tip portion 12 is covered or otherwise includes a sleeve 20 (as illustrated in
As noted above the distal or tip portion 12 can further comprises a sleeve or cover 20 as illustrated in
In various embodiments, the sleeve 20 comprises one or more layers of one or more monofilament braids, one or more layers of a plurality of interwoven monofilament braids, and any combination thereof. In various embodiments, the sleeve 20 comprises a first layer of twenty-four interwoven monofilament braids covering or overlaying a second layer of twenty-four interwoven monofilament braids. In various embodiments, the layers and/or the plurality of braids of one or more of the layers are interwoven together to create a pattern such as a lattice work, a generally diamond shape, or similarly shaped openings. In various embodiments, the pattern creates or provides openings or passages between the layers of the interwoven braids. In various embodiments, the openings or passages between the layers of the interwoven braids provide access or passageways to the distal or tip portion 12 of the shaft.
In various embodiments, the sleeve 20 covers or is otherwise attached to the distal or tip portion 12 of the shaft. In various embodiments, the distal or tip portion 12 of the shaft comprises one or more protrusions and one or more apertures and/or through-holes. In various embodiments, the distal or tip portion 12 of the shaft has a diameter greater than a proximal end or proximal portion of the shaft. In various embodiments, the distal or tip portion 12 of the shaft has a shape that delimits or provides an outer profile or periphery of a generally oval or oblate shape. In various embodiments, the middle portion or near the middle portion of the distal or tip portion 12 of the shaft has or delimits a diameter greater than the outer diameter of the shaft.
In various embodiments, the sleeve 20 forms an enclosure encompassing the distal or tip portion 12 of the shaft. In various embodiments, the sleeve 20 comprises one or more layers of braided monofilaments. The sleeve 20 may have a tip that is formed using heat. In particular the heat may be used to form the tip of the sleeve 20 or at least a closed end of the sleeve 20. Tipped layers of the sleeve 20 are slipped over the distal or tip portion 12 of the shaft through an opposing or open end of the sleeve 20. The open end of the sleeve 20 is then attached to the shaft, for example using an adhesive such as UV-cured glue.
In various embodiments, as illustrated in
In various embodiments, the break portion 14 is an attachment area or portion releasably coupling the distal or tip portion 12 to the handle portion 16 of the shaft. In various embodiments, a subsequent distal or tip portion 12 may be releasably attached to the handle portion 16 of the shaft.
In various embodiments, the collection swab length and diameter (i.e., geometry) allows for sufficient access to the desired specimen collection location. In various embodiments, the diameter of the portion between the handle portion 16 and the distal or tip portion 12 allows for bending to navigate the anatomy to access the desired collection location where the desired specimen may be located. In various embodiments, the break portion 14 allows for separation of the distal or tip portion 12 of the shaft associated with the collection swab 10 to be placed in a specimen collection container 30. In various embodiments, the break portion 14 facilitates a clean break of the distal or tip portion 12 of the shaft without additional fragments. In various embodiments, the break portion 14 and/or shaft of the collection swab 10 is made of polystyrene thereby facilitating in the clean break of the break portion 14.
In various embodiments, the distal or tip portion 12 has a geometry and associated sleeve 20 (e.g., braided layers) that facilitates in collecting samples or fluid collection by adsorption. Sample retrieval, in various embodiments, is also facilitated by the selection of hydrophobic materials of at least the distal or tip portion 12 and sleeve 20. For example, polystyrene and polyester are considered generally hydrophobic. Therefore, in accordance with various embodiments, the materials of the distal or tip portion 12 and sleeve 20 do not interact with the sample. Because the sample fluids are not being absorbed into the distal or tip portion 12 and/or sleeve 20 material, there is minimal or no concern of sample contamination at the time of sample collection.
In various embodiments, the spacing or gaps between the filaments (e.g., monofilaments) and/or the overlapping filaments delimiting the sleeve 20 and making up a sleeve surface and/or the voids in the geometry of the distal or tip portion 12 that causes the adsorption, capillary, and/or capture effect. The spacing or gaps between the filaments (e.g., the braided monofilaments lattice) of the sleeve 20 also allows for the fluid or sample to be adsorbed into the voids created in the distal or tip portion 12 geometry (e.g., protrusions, apertures, and the like). The underlying geometry of the distal or tip portion 12 is also configured such that the distal or tip portion 12 will not cause fluid or air to be trapped, such as in pockets, as the adsorption effect is advancing the fluid in the distal end through the openings or gaps between the monofilaments of the sleeve 20.
In various embodiments, the collection swab 10 provides an uptake volume of the fluid or specimen of about 20-100 uL. In various embodiments the collection swab 10 can also provide an uptake volume of the fluid or specimen of at least 100 uL and as high as 150 uL. In various embodiments, the uptake rate and/or volume can be varied by the sub structure of the distal or tip portion 12, for example by doing one or more of the following: varying the number, size, and shape of the voids in the sub structure and/or the sleeve 20, varying the spacing or gaps between the voids, the number, size and shape of each of the voids, varying the voids between the filaments and/or layers and/or the number, size and shape of overlapping layers associated with the sleeve 20. In various embodiments, the uptake rate and/or volume can be varied by the distance or space between the sleeve 20 and the sub structure of the distal or tip portion 12. In various embodiments, the uptake rate and/or volume can be varied by any combination of the above.
The combined underlying structure associated with the distal or tip portion 12 and braided layer(s) or sleeve(s) 20, in various embodiments, are also configured to facilitate sufficient release of the specimen or fluid for the same aforementioned reasons in regards to the hydrophobic nature of the material and the openings, spacing or gaps between or defined or delimited by the filaments of the layer(s) or sleeve(s) 20 as the distal or tip portion 12 geometry facilitates free flow of fluid having no pockets to trap fluid after it is placed in the sample container and vortexed for retrieval of the specimen for testing.
The combined underlying structure associated with the distal or tip portion 12 of the shaft and the braided covering or sleeve 20 in various embodiments is configured to not cause damage or irritation to the anatomy at the sample location. In accordance with various embodiments, the materials chosen allows for sterilization (e.g., with the use of e-beam, gamma, or the like). In various embodiments, the shaft of the collection swab 10 is made of polystyrene, the sleeve 20 is made of a polyester monofilament. Furthermore, a UV-cured glue can be used to connect the sleeve 20 and the shaft of the collection swab 10 together.
In accordance with various embodiment, the collection swab 10 is inserted into a patient's nasal cavity, ensuring that the area between the distal or tip portion 12 and the break portion 14 or intermediary portion is not touched during handling. The collection swab 10 is rotated to collect the sample, ensuring the distal or tip portion 12 only touches the suspected infections area to minimize potential contamination. After the specimen collection is completed, the collection swab 10 is placed into the collection container 30 and in various embodiments, a portion of the collection swab 10 is broken at the designated break portion 14. In accordance with various embodiments, the collection swab 10 may also be used as an applicator to collect a specimen in the same or similar fashion at other various anatomical locations.
In accordance with various embodiments, the collection systems described herein provide a sufficient or particular uptake volume of specimen (e.g., 20 uL-150 uL) or uptake of fluid in the distal or tip portion 12 of the shaft associated with the collection swab 10. In various embodiments, the collection swab 10 comprises of materials that does not interfere with diagnostic testing (e.g., Polymerase Chain Reaction Test) and/or may be sterilized. In accordance with various embodiments, the collection swab 10 provides efficient release of sufficient sample or fluid once the collection swab 10 is placed into the collection container 30. The collection container 30, in various embodiments, is vortexed with the collection swab 10 or portions thereof present to release the sample prior to the collection swab 10 removal from the collection tube 30. In accordance with various embodiments, the distal or tip portion 12 of the shaft associated with the collection swab 10 is atraumatic or does not cause irritation to the patient at the location where the specimen is taken.
In various embodiments, the sleeve 20 is position loosely around the distal or tip portion 12 of the shaft providing a gap to allow capture and subsequent release of the specimen. In accordance with various embodiments, the sleeve 20 and distal or tip portion 12 of the shaft is configured to provide an adsorption, capillary, and/or capture effect to collect the sample. In various embodiments, the pattern or gaps provided within the sleeve 20, distal or tip portion 12, gaps or spacing therebetween, or various combinations thereof provide an adsorption and capture effect to collect the tissue. In various embodiments, the pattern or gaps provided within the sleeve 20, distal or tip portion 12, gaps or spacing therebetween or various combinations thereof provide passageways to allow the complete or sufficient release or free passage of the specimen away from the distal or tip portion 12 of the shaft.
In accordance with various embodiments, the collection swab 10 comprises differing numbers of filaments (e.g., monofilaments), single or numerous filament layers, or any combinations thereof. In various embodiments, the sleeve 20 is attached by heat staking, adhesives, or the like, shrink tubing, or other mechanical attachments. In accordance with various embodiments, the collection swab 10 comprises a shaft with a single injection molded geometry without a sleeve. In accordance with various embodiments, the collection swab 10 comprises a shaft and one or more sleeves 20. In various embodiments, the collection swab 10 comprises one or more sleeves 20 being different or the same and/or be made of an absorbent material. In various embodiments, the distal or tip portion 12 is configured to have tiered type geometry as shown for example in
With reference to each of the figures in this application, a cover or sleeve (hereinafter referred to as a cage) are illustrated in accordance with various embodiments of the invention. The cage 20 is adhered to, mechanically snapped onto, or otherwise attached to the shaft of the collection swab. In various embodiments, the cage and shaft of the collection swab are integrated forming a monolithic structure. The shaft in various embodiments includes a distal or tip portion, inner geometry, extension, or post with a specified geometry including one or more projections, protrusions, ribs, apertures, divots, thru-holes (herein generally referred to as “apertures”) and/or various combinations thereof. In various embodiments, the projections, protrusions and/or ribs are curved or generally arcuate to maximize surface area for specimen/tissue collection and/or avoid traumatic contact with the collection site and/or the cage. As seen in the
In various embodiments, the protrusions 32 associated with the distal or tip portion are generally uniform in height and in spacing therebetween (see
In various embodiments, the cage includes one or more panels, ribs, and/or braids. These features are capable of providing a specific operational or clinical outcome such as a desired capture or adsorption rate, retention, and/or release, and/or ease operation or manufacturing processes. Similarly, in various embodiments, the cage includes one or more spaces or openings and provides a specific operational or clinical outcome such as a desired capture or adsorption rate, retention and/or release, and/or ease operation or manufacturing processes. In various embodiments, as shown for example, in
In various embodiments, outer surface or surfaces of the panel, rib, braid, or combinations thereof are arranged to contact the desired patient's area and in particular contact the desired specimen or tissue such that the specimen/tissue collects and travels along the outer surface and/or ingress through the spaces or openings defined by a pattern or layout of the arranged panels, ribs, and/or braids, and/or between consecutive panels, ribs, and/or braids. As such, in various embodiments, the one or more spacings or openings between the one or more panels, ribs, braids, or any combination thereof, provides access of the ingress of the tissue or specimen within the confines or coverings delimited by the cage and is temporarily entrapped or captured within the confinement, the extension, or both. Likewise, the spacing or opening between the ribs, braid, or braids provide eventual egress of the tissue or specimen upon retrieval by vortex mechanisms, or the like for diagnostic or testing purposes. As such, in accordance with various embodiments, as shown for example throughout the figures, the one or more panels, ribs, braids, or combinations thereof and/or spaces or openings defined thereby can vary in number, size, alignment and/or shape and/or disposed along all, some or in clumps, with spacing therebetween uniform and/or varied, as desired to provide a specific operational or clinical outcome, e.g., desired capture or adsorption rate, temporary retention and/or release and/or ease operation or manufacturing processes.
In accordance with various embodiments, as shown for example throughout the figures, the one or more protrusions, projections, or ribs can vary in number, size, alignment and/or shape and/or disposed along all, some or in clumps, with spacing therebetween uniform and/or varied, as desired to provide a specific operational or clinical outcome, e.g., desired capture or adsorption rate, retention and/or release, reducing or eliminating air traps and/or supporting the cage, and/or ease operation or manufacturing processes. Likewise, the projections, protrusions or ribs are spaced or abut portions of the cage and/or are disposed within the spaces or openings of the cage. Similarly, the apertures, divots and/or thru-holes can vary in number, alignment, size and/or shape as desired to provide a specific operational or clinical outcome, e.g., desired capture or adsorption rate, retention and/or release and/or reducing or eliminating air traps, and/or ease operation or manufacturing processes.
In various embodiments, the post or extension 30 may extend from a support or bolster 40. The bolster 40 is an enlarged portion at the distal end of the shaft and provides a support or attachment useful or assisting in the connection of the cover, sleeve or cage to the shaft. The bolster 40 in various embodiments includes one or more channels or cutouts 42 disposed around the periphery of the bolster to provide a snap connection or mating connection with one or more projections or tabs extending from a proximal end of the cage and similarly disposed around the periphery of the cage. In various embodiments, the cage provides the one or more cutouts or channels 211 and the bolster provides the one or more tabs or projections 44 or either provides combinations thereof. In various embodiments, protrusions 301 engage, snap or otherwise connect the cage within spaces between the ribs 206. In various embodiments, the cage comprises a proximal support ring having the one or more cutouts, channels, tabs, projections, or any combination thereof to mate with their like counterpart of the bolster. In various embodiments, the support ring includes one or more slots or apertures to provide a path or inlet for adhesive to be added to enhance the connection of the cage to the shaft. In various embodiments, the bolster provides a generally flat surface to provide a stable or uniform connection for the attachment of the cage. In various embodiments, the flat surface, channel, or protrusions include adhesive or the like to connect or bond the cage to the bolster 40. In accordance with various embodiments, an extension does not extend from the bolster 40 and as such the cage 20 encompasses or delimits an empty space, as shown for example in
In various embodiments, the cage generally defines a cylindrical shape with an enclosed rounded or blunt tip. In various embodiments, the cage is flexible or elastic deformable to contact one or more of the protrusions of the extension, reducing potential discomfort or trauma at the collection site. In various embodiments, the cage is a cylindrical cover having one or more apertures, openings, or slots 212 therethrough as shown for example in
In the figures present in the application, various views of various embodiments of the cover, sleeve, cage 20 and/or distal portion of the shaft, extension or post along with various combinations thereof are shown. It should be noted that although various combinations are shown in these figures and described throughout the application, different embodiments of the sleeve/cage 20 and/or extension/post can be interchanged, combined and/or replaced to provide a desired operational outcome, e.g., desired capture or adsorption rate, retention and/or release, and/or ease operation or manufacturing processes. In accordance with various embodiments described throughout and various combinations thereof, collection swabs are described in which the distal portion of the shaft, extension or post provides inner swab geometry or structures and/or the cover, sleeve, cage provides an outer swab geometry or structures.
In various embodiments, the combination of the inner and outer geometry/structure, including the lack of one or the other, a balance is maintained or provided between specimen/tissue/fluid adsorption or capture volume and/or rate, along with air displacement, e.g., avoiding or removing air traps, and temporary specimen/tissue/fluid retention. In accordance with various embodiments and combinations thereof, the collection swab and in particular, the distal portion of the shaft, extension or post and/or the cover, sleeve and/or cage are made of material that has adsorptive properties but no or negligible absorptive properties (e.g., unlike a cotton swab) and as such facilitates ultimate release and/or retrieval of specimen/tissue/fluid for diagnostics and/or testing. In accordance with various embodiments and combinations thereof, proximal or handle portions of the collection swab as described throughout and/or unfeatured shafts, may be attached, structurally, mechanically, adhered or otherwise connected to the various embodiments and combinations thereof of the distal portion of the shaft, extension or post and/or the cover, sleeve and/or cage 20.
In the following sections, further details will be provided for each of the various embodiments alluded to above. In particular, the various embodiments, as discussed in
With respect to
With reference to
With the particular shape, as illustrated in the figure, the protrusions of the collection swab can be used to scrape/collect the specimen/tissue/fluid from the desired area (e.g., nasal cavity) of the patient as the collection swab is inserted into the desired area and/or moved around in the desired area. The specimen/tissue/fluid that are obtained from the protrusions can then be deposited within the grooves between each of the protrusions of the collection swab. When the collection swab is removed, the specimen/tissue/fluid is removed from the desired area.
As discussed above, the specimen/tissue/fluid collected via the collection swab can then be stored (along with part or the entirety of the collections swab) within a collection container. As discussed above, the collection container provides a secure/safe means of carrying the specimen/tissue/fluid as it is being transported or at least until the specimen/tissue/fluid can be used (e.g., testing).
Next,
The distal or tip portion may have a number of protrusions 32 with some or all of the protrusions having a through-hole located at the outer-most tip of the protrusion. There may also be additional apertures 34 located at the distal or tip portion positioned between the protrusions 32. In addition protrusions may also be located at the distal most point of the shaft 38.
Each of the protrusions and/or apertures 32, 34, 38 are configured to facilitate in the collection of specimens/tissues/fluids when the collection swab is inserted into a desired location. A benefit for the through-holes associated with the protrusions 32 may be to allow for the breaking of surface tensions as the collection swab is inserted and maneuvered within the desired location (e.g., nasal cavity). Furthermore, the through-holes may also provide benefits during the collection (e.g., absorption) and retaining of the specimen/tissue/fluid as the specimen/tissue/fluid may be captured within the protrusions 32. The specimen/tissue/fluid can be stored within the protrusions 32 until removed at a later time, for example, via the use of centrifugal force or by shaking the collection swab to dislodge the specimen/tissue/fluid from the protrusions.
As discussed above, the sleeve or cage can be used to facilitate in the collection of specimen/tissue/fluid from the desired location (e.g., nasal passage). In
As the collection swab with the sleeve or cage is inserted and maneuvered in the desired location, it may be possible to dislodge and subsequently collect specimen/tissue/fluid as the surface of the sleeve or cage come into contact with the desired location. The sleeve or cage may be capable of retaining some of the specimen/tissue/fluid after collecting from the desired location. The sleeve or cage may have features or be made of materials that allow for the specimen/tissue/fluid to be retained by the sleeve or cage. In some cases, the specimen/tissue/fluid may also be pulled into the interior of the sleeve or cage thereby coming into contact with the distal or tip portion of the shaft associated with the collection swab (if present). The specimen/tissue/fluid may then attach itself to the distal or tip portion and be retained within the sleeve or cage in this manner as well.
The sleeve/cage can be used as a way to retain and transport the specimen/tissue/fluid collected from a patient. When the specimen/tissue/fluid is ready to be retrieved for use (e.g., testing), a user may use centrifugal force or by shaking the collection swab to dislodge the specimen/tissue/fluid from the sleeve or cage.
Turning now to
With respect to
With respect to
In some embodiments, the sleeve or cage can be formed via molding as a single monolithic device along with the distal or tip portion (see
With respect to
In addition, the distal or tip portion of the shaft associated with the collection swab has a different design involving a number of protusions 32 which are circular. These protrusions 32 are spaced apart from each other along the length of the distal or tip portion. In this way the protrusions 32 can be used to scrape or dislodge specimen/tissue/fluids from a desired location as the collection swab is inserted and maneuvered at the desired location. The space between the protrusions 32 could be used to retain/absorb/capture the specimen/tissue/fluids when the collection swab is removed.
What differs from the embodiments illustrated in the figures compared to the other embodiments discussed so far is with the distal or tip portion of the shaft associated with the collection swab. In particular, the distal or tip portion can be seen as having a distal portion associated with the protrusions while the proximal portion of the distal or tip portion is left bare (e.g., no protrusions are provided here). Rather, additional elements are added near the bolster 40 which are directed to allow for the attachment of a sleeve or cage to the distal or tip portion. For example, a channel or cutout 42 can be disposed around the bolster 40 which could provide a more secure fit between the sleeve or cage and the distal or tip portion. Furthermore, the connection between the sleeve or cage within the channel or cutout 42 could operate as a seal thereby providing a more secure way to retain specimen/tissue/fluid collected via the collection swab. The proximal support ring could have apertures or other features that would allow for the sleeve or cage to engage with the bolster 40 and/or channel or cutout 42 to assist in the connection and seal between the sleeve or cage and the distal or tip portion of the shaft.
As described above, the sleeve or cage can snap connect with the distal or tip portion of the shaft. Adhesives can also be used in order to secure the two elements together as well as provide a seal therebetween.
These variations of the collection swab may be used if the sleeve or cage is designed to collect and retain the specimen/tissue/fluid, there may not be a need for a distal or tip portion. Thus, by removing the unnecessary portion of the collection swab, this can simplify the manufacture of the collection swab.
Different size ribs are also used based on the location along the sleeve or cage. Smaller and thinner ribs can be used at the distal end of the sleeve or cage in order to provide the ability of the sleeve or cage to flex and bend as the collection swab is inserted and navigated within the desired location. Meanwhile thicker ribs can be used at the proximal end of the sleeve or cage in order to provide a more sturdy foundation as the sleeve or cage flexes or bends. Other methods of allowing for flexibility/sturdiness for the sleeve or cage can also be realized based on the reduction in the number of support/braces implemented (see the third variations in
The above description is provided to enable any person skilled in the art to make and use the devices or systems and perform the methods described herein and sets forth the best modes contemplated by the inventors of carrying out their inventions. Various modifications, however, will remain apparent to those skilled in the art. It is contemplated that these modifications are within the scope of the present disclosure. Different embodiments or aspects of such embodiments may be shown in various figures and described throughout the specification. However, it should be noted that although shown or described separately each embodiment and aspects thereof may be combined with one or more of the other embodiments and aspects thereof unless expressly stated otherwise. It is merely for easing readability of the specification that each combination is not expressly set forth.
Although the present invention has been described in certain specific aspects, many additional modifications and variations would be apparent to those skilled in the art. It is therefore to be understood that the present invention may be practiced otherwise than specifically described, including various changes in the size, shape and materials, without departing from the scope and spirit of the present invention. Thus, embodiments of the present invention should be considered in all respects as illustrative and not restrictive.
The present application claims the priority benefit of U.S. provisional patent application 63/026,393 filed May 18, 2020 and U.S. provisional patent application 63/012,075 filed Apr. 17, 2020, the disclosures of which are incorporated herein by reference.
Number | Date | Country | |
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63012075 | Apr 2020 | US | |
63026393 | May 2020 | US |