Abstract: An apparatus includes a body, a flexible cannula, and a needle. The needle is resiliently biased to extend along at least one proximal curve through least one proximal curved needle portion. The needle is resiliently biased to extend along at least one distal curve through at least one distal curved needle portion. In another embodiment, an apparatus includes a main body portion including a proximal channel configured to receive a plunger of a syringe, and a stop surface configured to selectively engage the plunger of the syringe to arrest distal advancement of the plunger. The apparatus also includes first and second deflectable beams configured to cooperate with each other to securely grip the barrel of the syringe, and first and second deflectable flanges configured to cooperate with each other to grip the barrel of the syringe.

Abstract: A drive apparatus fits into a storage cabinet with a storage unit with shelves and is suited for mounting on a wall above a worktop. A push/pull mechanism pushes the storage unit outwardly from the housing, and a separate vertical drive mechanism then lowers the storage unit to a level beneath the housing, where it is accessible. Because the storage unit is initially pushed outwardly to a to extended position, when it is lowered it does not impact on items directly underneath the cabinet. Hence the cabinet may be fitted in a conventional arrangement. A door drive mechanism allows automated opening and closing of the doors, but if they are opened manually the drive mechanism remains disengaged. Upon automated door closure the door mechanism disengages when nearly closed due to the mutual physical arrangement of the mechanism components, thereby allowing the door's own soft hinge to complete the door closure, thereby avoiding pinch points and allowing the next door opening to be either manual or automated.

Abstract: An apparatus includes a body, a flexible cannula, and a needle. The cannula is sized and configured to advance between a sclera and a choroid of a patient's eye. The needle is slidably disposed in the cannula and includes a sharp distal tip. The needle translates relative to the cannula between a proximal position and a distal position. The distal tip is positioned inside the cannula when the needle is in the proximal position. The distal tip is positioned outside the cannula when the needle is in the distal position. The needle is resiliently biased to extend along at least one proximal curve through least one proximal curved needle portion. The needle is resiliently biased to extend along at least one distal curve through at least one distal curved needle portion. The at least one distal curve is different from the at least one proximal curve.

Abstract: Methods, apparatus, systems, computing devices, computing entities, and/or the like for identifying one or more visual impairments of a user, mapping the visual impairments to one or more accessibility solutions, (e.g., program code entries) and dynamically modifying a display presentation based at least in part on the identified accessibility solutions.

Abstract: A drive apparatus fits into a storage cabinet with a storage unit with shelves and is suited for mounting on a wall above a worktop. A push/pull mechanism pushes the storage unit outwardly from the housing, and a separate vertical drive mechanism then lowers the storage unit to a level beneath the housing, where it is accessible. Because the storage unit is initially pushed outwardly to a to extended position, when it is lowered it does not impact on items directly underneath the cabinet. Hence the cabinet may be fitted in a conventional arrangement. A door drive mechanism allows automated opening and closing of the doors, but if they are opened manually the drive mechanism remains disengaged. Upon automated door closure the door mechanism disengages when nearly closed due to the mutual physical arrangement of the mechanism components, thereby allowing the door's own soft hinge to complete the door closure, thereby avoiding pinch points and allowing the next door opening to be either manual or automated.

Abstract: Methods, apparatus, systems, computing devices, computing entities, and/or the like for identifying one or more visual impairments of a user, mapping the visual impairments to one or more accessibility solutions, (e.g., program code entries) and dynamically modifying a display presentation based at least in part on the identified accessibility solutions.

Abstract: Methods, apparatus, systems, computing devices, computing entities, and/or the like for identifying one or more visual impairments of a user, mapping the visual impairments to one or more accessibility solutions, (e.g., program code entries) and dynamically modifying a display presentation based at least in part on the identified accessibility solutions.

Abstract: An absorption chiller includes a boiler with a vessel for storing a working fluid and a heat source configured to heat the working fluid. A first device is configured to cool the working fluid, and a second device is configured to cool the working fluid. A flow path is arranged to enable the working fluid to flow from the boiler through the first device, through the second device and back to the boiler. A first waste heat source is generated by the first device when cooling the working fluid. The first waste heat source is configured to heat the working fluid along the flow path after exiting the second device and prior to re-entering the boiler.

Abstract: Methods, apparatus, systems, computing devices, computing entities, and/or the like for identifying one or more visual impairments of a user, mapping the visual impairments to one or more accessibility solutions, (e.g., program code entries) and dynamically modifying a display presentation based at least in part on the identified accessibility solutions.

Abstract: A solid oxide fuel cell comprising a cathode, an electrolyte, a functional layer and an anode support. The anode support comprises A-B-C: A is a nitrate, an oxide, a salt or a carbonate selected from the group of: alkali, alkaline oxide, alkaline earth metal or combinations thereof, B is selected from the group of: Fe, Ni, Cu, Co or combinations thereof, and C is selected from the group of: PSZ, YSZ, SSZ, SDC, Ce doped SSZ, GDC or combinations thereof. In the solid oxide fuel cell A ranges from about 0 to about 20 wt % of the anode support, B ranges from about 0.1 to about 70 wt % of the anode support and C ranges from about 0.1 to about 60 wt % of the anode support.

Abstract: An absorption chiller includes a boiler with a vessel for storing a working fluid and a heat source configured to heat the working fluid. A first device is configured to cool the working fluid, and a second device is configured to cool the working fluid. A flow path is arranged to enable the working fluid to flow from the boiler through the first device, through the second device and back to the boiler. A first waste heat source is generated by the first device when cooling the working fluid. The first waste heat source is configured to heat the working fluid along the flow path after exiting the second device and prior to re-entering the boiler.

Abstract: In general, techniques are described for labeling an implantable medical device (IMD). In one example, an IMD can include a housing including electronic circuitry. The IMD can include a header coupled to the housing and includes a core. The core can define a bore and include a first metal label positioned adjacent to the at least one bore. The IMD includes a lead assembly including at least one lead having a distal end and a proximal end, the at least one lead including a second metal label, the distal end including at least one electrode and the proximal end received within the bore.

Abstract: The present invention provides an apparatus for suture-based tissue repair, preferably for the annulus of a spinal disc, that includes a suture loop preferably pre-tied with a sliding knot, a clasp-type component that captures the ends of the suture loop, and an optional plug member that fills the tissue defect. Also disclosed is a method that places the suture loop in a full-thickness stitch encircling the tissue defect, secures the ends of the suture loop to the clasp, and cinches the suture loop to approximate the tissue without the need to tie knots. Also disclosed is a suture passer that enables a suture strand or loop to be passed through the tissue wall, captured, and retrieved. The suture passer may optionally incorporate a clasp in such an arrangement that enables a suture loop passed through the tissue wall to be captured directly by the clasp.

Abstract: In general, techniques are described for labeling an implantable medical device (IMD). In one example, an IMD can include a housing including electronic circuitry. The IMD can include a header coupled to the housing and includes a core. The core can define a bore and include a first metal label positioned adjacent to the at least one bore. The IMD includes a lead assembly including at least one lead having a distal end and a proximal end, the at least one lead including a second metal label, the distal end including at least one electrode and the proximal end received within the bore.

Abstract: In general, techniques are described for labeling an implantable medical device (IMD). In one example, an IMD can include a housing including electronic circuitry. The IMD can include a header coupled to the housing and includes a core. The core can define a bore and include a first metal label positioned adjacent to the at least one bore. The IMD includes a lead assembly including at least one lead having a distal end and a proximal end, the at least one lead including a second metal label, the distal end including at least one electrode and the proximal end received within the bore.

Abstract: A solid oxide fuel cell comprising a cathode, an electrolyte, a functional layer and an anode support. The anode support comprises A-B-C: A is a nitrate, an oxide, a salt or a carbonate selected from the group of: alkali, alkaline oxide, alkaline earth metal or combinations thereof, B is selected from the group of: Fe, Ni, Cu, Co or combinations thereof, and C is selected from the group of: PSZ, YSZ, SSZ, SDC, Ce doped SSZ, GDC or combinations thereof. In the solid oxide fuel cell A ranges from about 0 to about 20 wt % of the anode support, B ranges from about 0.1 to about 70 wt % of the anode support and C ranges from about 0.1 to about 60 wt % of the anode support.

Abstract: A method of forming and the resulting membrane composition for securement to a patient's bone or tissue to reduce the formation of tissue adhesions following a surgical procedure comprises a first component and a second component. The first component comprises a hydrogel including at least one crosslinked polymer. The second component comprises a textile component. The composition has a thickness between about two tenths of a millimeter (0.2 mm) to about six tenths of a millimeter (0.6 mm), a suture retention strength between about one Newton (1 N) to about thirteen Newtons (13 N), a static coefficient of friction between about one hundredth (0.01) and about one-half (0.5), a kinetic coefficient of friction between about one hundredth (0.01) and about one-half (0.5) and a flexibility of less than thirty millimeters (30 mm) bend length. A method of reducing the occurrence of tissue adhesions following surgery comprises applying the membrane composition to a surgical site.

Abstract: In general, techniques are described for labeling an implantable medical device (IMD). In one example, an IMD can include a housing including electronic circuitry. The IMD can include a header coupled to the housing and includes a core. The core can define a bore and include a first metal label positioned adjacent to the at least one bore. The IMD includes a lead assembly including at least one lead having a distal end and a proximal end, the at least one lead including a second metal label, the distal end including at least one electrode and the proximal end received within the bore.

Abstract: A method of forming and the resulting membrane composition for securement to a patient's bone or tissue to reduce the formation of tissue adhesions following a surgical procedure comprises a first component and a second component. The first component comprises a hydrogel including at least one crosslinked polymer. The second component comprises a textile component. The composition has a thickness between about two tenths of a millimeter (0.2 mm) to about six tenths of a millimeter (0.6 mm), a suture retention strength between about one Newton (1 N) to about thirteen Newtons (13 N), a static coefficient of friction between about one hundredth (0.01) and about one-half (0.5), a kinetic coefficient of friction between about one hundredth (0.01) and about one-half (0.5) and a flexibility of less than thirty millimeters (30 mm) bend length. A method of reducing the occurrence of tissue adhesions following surgery comprises applying the membrane composition to a surgical site.

Abstract: A method of forming and the resulting membrane composition for securement to a patient's bone or tissue to reduce the formation of tissue adhesions following a surgical procedure comprises a first component and a second component. The first component comprises a hydrogel including at least one crosslinked polymer. The second component comprises a textile component. The composition has a thickness between about two tenths of a millimeter (0.2 mm) to about six tenths of a millimeter (0.6 mm), a suture retention strength between about one Newton (1 N) to about thirteen Newtons (13 N), a static coefficient of friction between about one hundredth (0.01) and about one-half (0.5), a kinetic coefficient of friction between about one hundredth (0.01) and about one-half (0.5) and a flexibility of less than thirty millimeters (30 mm) bend length. A method of reducing the occurrence of tissue adhesions following surgery comprises applying the membrane composition to a surgical site.