A surgical instrument comprises a body, a transmission assembly, and a switch. The body comprises a control unit and an integral power source. The power source is operable to selectively deliver power to the control unit. The transmission assembly extends distally from the body. The transmission assembly also includes an end effector driven by the control unit. The switch is in communication with the control unit and the power source. The transmission assembly is operable to actuate the switch to enable delivery of power from the power source to the control unit.

A sterile case for an electronic device used during medical procedures includes a rigid housing with at least one transparent face. An opening in the housing permits movement of the device into and out of the housing in, for example, a direction parallel to the length or width of the housing. A door attached to the housing moves between open and closed positions to seal the opening. A sleeve is configured to be received, when the door is in the open position, partially within the housing and to extend outward from the housing through the opening. The sleeve defines a bore aligned with the opening and configured to receive the device and to permit insertion of the device through the sleeve into the housing without contact between the device and a rim of the housing surrounding the opening.

An allergy testing kit contains a plurality of allergy testing applicators, an allergy testing tray and a plurality of allergen bottles each containing an allergen. Each of the applicators contains an elongated handle, a plurality of arms extending from the elongated handle and disposed in an asymmetrical configuration, and a plurality of legs with tines extending from each of the arms. The allergy testing tray contains a main body having an underside and a top surface, a cover for locking with the main body and a plurality of reservoirs extending from the underside of the main body. The reservoirs each have a chamber with an opening extending from the top surface. The reservoirs are disposed in different groups and each group has an asymmetrical configuration matching that of the applicator.

A syringe assembly includes (1) a syringe barrel defining a chamber; (2) a plunger mounted in the chamber and moveable with respect to the barrel; and (3) a cap assembly containing a cap and an absorbent material is removably attached to the plunger. A strip package includes at least two cap assemblies. Each of the cap assemblies includes a cap holder and an antiseptic cap positioned in the cap holder. The antiseptic cap includes a sidewall defining a chamber and an antiseptic substance within the chamber. A strip extends over at least two cap assemblies. The strip includes a first seal engaged to the cap holder and a second seal engaged to the antiseptic cap.

A carrying case (500) and handle (504) for accommodating a portable topical negative pressure therapy apparatus (200) comprising a device (202) and a waste canister (204) separable therefrom, the waste canister having an aspiration conduit (274) emerging therefrom is described, the carrying bag comprising an apparatus receiving pouch (502), said pouch having opening and closing means (522, 524) at a lower portion thereof and said handle (504) being directly attached to said apparatus.

A sterile case for an electronic device used during medical procedures includes a rigid housing with at least one transparent face. An opening in the housing permits movement of the device into and out of the housing in, for example, a direction parallel to the length or width of the housing. A door attached to the housing moves between open and closed positions to seal the opening. A sleeve is configured to be received, when the door is in the open position, partially within the housing and to extend outward from the housing through the opening. The sleeve defines a bore aligned with the opening and configured to receive the device and to permit insertion of the device through the sleeve into the housing without contact between the device and a rim of the housing surrounding the opening.

A sheath for an oximetry device includes a top and a body where the top opens to provide an opening where the oximetry device can be placed into the body of the sheath. The top of the sheath can be closed onto the body and the closure of the top can be verified by circuits in the oximetry device. The circuits can monitor the position of a latch that is connected to the top of the sheath. The circuits can determine when the latch is unlatched and the top is open and not sealed closed to the body. And, the circuits can determine when the latch is latched and the top is closed and sealed to the body.

A syringe assembly includes (1) a syringe barrel defining a chamber; (2) a plunger mounted in the chamber and moveable with respect to the barrel; and (3) a cap assembly containing a cap and an absorbent material is removably attached to the plunger. A strip package includes at least two cap assemblies. Each of the cap assemblies includes a cap holder and an antiseptic cap positioned in the cap holder. The antiseptic cap includes a sidewall defining a chamber and an antiseptic substance within the chamber. A strip extends over at least two cap assemblies. The strip includes a first seal engaged to the cap holder and a second seal engaged to the antiseptic cap.

A sheath for an oximetry device includes a top and a body where the top opens to provide an opening where the oximetry device can be placed into the body of the sheath. The top of the sheath can be closed onto the body and the closure of the top can be verified by circuits in the oximetry device. The circuits can monitor the position of a latch that is connected to the top of the sheath. The circuits can determine when the latch is unlatched and the top is open and not sealed closed to the body. And, the circuits can determine when the latch is latched and the top is closed and sealed to the body.

An apparatus includes a plurality of beads, and a linking assembly. Each bead in the plurality of beads includes at least one magnet and a unibody housing encasing and sealing the at least one magnet. The unibody housing includes a magnetically inert material being formed of a particulate powder composition. The linking assembly joins the beads together such that the beads and the linking assembly in arranged in an annular arrangement sized to form a loop around an anatomical structure of a patient. The loop may transition between a contracted configuration and an expanded configuration while being magnetically biased toward the contracted configuration by a magnetic bias of the beads.