Abstract: The present invention relates to a control method of a wheel alignment apparatus using an MDPS, which determines whether or not to cancel center alignment control due to a trouble or error is preferentially determined prior to each control step and then performs control when wheels of a vehicle having an MDPS mounted therein are aligned, such that the trouble or error is preferentially considered in the control priority, thereby increasing driver's convenience and improving safety performance for protecting the driver.

Abstract: An exemplary system for crimping a prosthetic valve comprises a radially expandable and compressible prosthetic valve, a crimping device positioned around the valve and configured to reduce the diameter of the valve to a delivery configuration, and a sterile package enclosing the valve and the crimping device. The valve can be pre-assembled in a partially crimped configuration within the crimping device. After removing the sterile packaging, the crimping device can be used to crimp the valve from the partially crimped configuration to the delivery configuration, such as by twisting a knob on the crimping device. The system can further comprise at least a portion of a delivery catheter within the sterile package, wherein the valve is pre-mounted on or adjacent to an inflatable balloon of the delivery catheter, such that the valve can be crimped onto the delivery catheter using the crimping device.

Abstract: The teachings herein provide a surgical instrument tray system comprising at least a stringer tray having an advantageous cradle configured to hold ring-handle instruments in a spaced-apart array. In particular, the cradle includes an array of compartments, with each compartment cradling and supporting the lower ring of a respective one of the ring-handle instruments loaded in the tray. Further, a removable, elongated locking member locks the lower rings within the cradle. These features allow the stringer tray to be used for neatly organizing and holding a potentially large quantity of ring-handle instruments, for presentation and use within an operating room environment, for stowage as part of a tracked tray system within a sterilization container, as well as to position and hold the ring-handle instruments in a fully open position for disinfecting and washing.

Abstract: Packaging for medical containers, including a tub having a peripheral wall, a sealing cover sealable on an opening of the tub and a sealing envelope able to protect the sealing cover. The sealing envelope includes: a lower sealing part, having a frame able to be sealed to the peripheral wall of the tub, and a bonding surface that extends outwards from the frame, and an upper sealing part sealed on the bonding surface to enclose the opening of the tub and the sealing cover.

Abstract: A protection system and method for use with surgical trays and to prevent a sterilization wrap around a sterilized surgical tray from being ripped, punctured, or torn is disclosed. The system includes at least one corner protector positioned on a respective corner of a surgical tray, and at least one edge guard positioned on a respective edge of the surgical tray. The at least one corner protector and at least one edge guard provide a cushion between the surgical tray and a sterilization wrap to prevent the wrap from being ripped, punctured, or torn.

Abstract: A surgical instrument caddy includes an elongated, generally rectangular main body having a support rod secured to one end and a plurality of hollow channels disposed therein. Each of the channels includes a first end terminating at the top surface of the main body, and a second end terminating at the bottom surface of the main body.

Abstract: A tray (100) for accommodating a coiled medical device, such as a catheter assembly (700), includes a first compartment (101), a second compartment (102), and a third compartment (103). The catheter assembly (700) and devices associated with a catheterization procedure, such as syringes (701,702) containing sterile water and lubricating jelly and a specimen container (703) can be disposed within the tray. A first barrier (105) and second barrier (106) separate the compartments. The barriers can have openings (121,122) therein to accommodate large syringes or to enable the first compartment (101) to be used as a lubricant applicator for the catheter. The first compartment (101) can include a stair-stepped contour (115) such that the syringes are held at different depths to facilitate ease of use. The various devices can be disposed within the tray (100) in accordance with their order of use in the catheterization procedure.

Abstract: A biological tissue cutting and fluid aspiration system provides a plurality of surgical instruments operable independent of an external control console. In some embodiments, each surgical instrument may include all sensors and controls directly applicable to the surgical instrument, and may be used independently. In some embodiments, instruments communicate status information to each other, and adjust operating parameters based on the communications.

Abstract: A non-reusable, locking container for sterilizing and storing surgical materials and presenting surgical materials in a sterilized condition. The non-reusable, locking sterilization container includes a tray, a lid, a permeable filter, a non-reusable lock and a frangible release that limit the container to only a single sterilization cycle or single use.

Abstract: A pharmaceutical waste disposal assembly (10) for disposing of one or more of fluid pharmaceutical waste and solid pharmaceutical waste includes a first waste receiver (614) and a receiver retainer (16). The first waste receiver (614) includes a first receiver body (621) having a first body access (621BA). Additionally, the pharmaceutical waste moves in a first direction (695C) toward the first body access (621BA) through which the pharmaceutical waste is directly received by the first receiver body (621). The receiver retainer (16) substantially encloses the first waste receiver (614). Further, the first waste receiver (614) is removable from the receiver retainer (16). Moreover, one of the first waste receiver (614) and the receiver retainer (16) includes a first waste guide (667A) that guides the pharmaceutical waste in a second direction (695A) away from the first body access (621BA) and in the first direction (695C) toward the first body access (621BA).

Abstract: Cassette for housing one or more medical instrument (18) including a tray having at least one passage (20) for receiving said medical instrument, said tray having a rigid structure (12) and a resilient holding means (28) arranged to retain the medical instrument (18) within said passage, wherein the holding means is located remote from the upper surface, and the at least one passage is formed by the rigid structure (12) and the holding means such that the uppermost section (44) of the passage is formed by the rigid structure and at least a portion of the lower section (46) of the passage is formed by the holding means.

Abstract: A support, a tray for surgical instruments and a method of manufacture are described. The support is used in a surgical tray to support surgical instruments and comprises a rigid part having a free end presenting a formation arranged to accept a part of a surgical instrument and a foot by which the support can be attached to a base of a surgical tray. The support is resiliently deformable so as to substantially return the support to an initial position if the support is knocked in use. The surgical tray includes can hold a plurality of surgical instruments, and comprises a body having walls defining an opening and a base, a lid engagable with the opening to close the tray and a plurality of supports extending from the base.

Abstract: An orthopedic fixation system includes a sterile packaged implant kit and a sterile packaged instrument kit. The sterile packaged implant kit includes at least one surgical implant, an insertion device, and an implant package adapted to receive the at least one surgical implant and the insertion device therein. The implant package maintains the at least one surgical implant and the insertion device sterile after sterilization of the sterile packaged implant kit. The sterile packaged instrument kit includes one or more instruments necessary to use the sterile packaged implant kit and an instrument package adapted to receive the one or more instruments therein. The instrument package maintains the one or more instruments sterile after sterilization of the sterile packaged instrument kit.

Abstract: A pharmaceutical waste disposal assembly (10) includes a receiver body (19), a receiver guide (62), a fluid absorber (70) and a fluid distributor (64). The receiver body (19) receives fluid pharmaceutical waste. The receiver guide (62) guides the fluid pharmaceutical waste into the receiver body (19). The fluid absorber (70) is positioned within the receiver body (19), and is adapted to absorb at least a portion of the fluid pharmaceutical waste that is received by the receiver body (19). The fluid distributor (64) is coupled to the receiver guide (62), and extends at least partially into the fluid absorber (70) so that the fluid distributor (64) distributes the fluid pharmaceutical waste within the fluid absorber (70). The fluid distributor (64) includes a plurality of distributor apertures (278) that allow the fluid pharmaceutical waste to flow from the receiver guide (62) to the fluid absorber (70).

Abstract: Systems and methods that process a plurality of surgical instruments for cleaning and/or packaging. A device identifies a robot-ready insert having a predetermined configuration for accepting at least one type of surgical instrument. The surgical instruments are identified and oriented according to type using an automated apparatus. Specialized tools are also provided for automatically opening and closing surgical instruments, flipping instruments and assisting in the processing and maintenance of surgical instruments. The automated apparatus then places each of the surgical instrument types in one or more predetermined areas of the insert, configured to accept a predetermined set of surgical instrument types.

Abstract: A sterilization system for sterilizing a surgical instrument includes a generally planar sterilization surface and a sterilization accessory disposed on the sterilization surface. The sterilization accessory is adapted to receive the surgical instrument thereon or therein, and the sterilization accessory is formed at least in part from an open cellular material. The open cellular material includes a generally planar base surface, a plurality of cells extending from the base surface, each of the plurality of cells including a side wall, which extends from the base surface, and an end wall. Each of the plurality of cells is open, such that gases surrounding the open cellular material are free to pass into and out of each of the plurality of cells.

Abstract: Disclosed is a combination medical case including multiple storage compartments, specifically for use by a diabetic patient. The medical case comprises a base compartment sized and shaped to contain a plurality of storage cubicles for the containment of prescription medicine bottles. The base compartment further contains a means for attachment of a planar-shaped equipment tray which may hold a glucose meter and a quantity of syringes or other supplies. A removable drawer, having a hinged top, rests on parallel supporting ledges integral to the inner walls of the base compartment. A shelf is sized and shaped to horizontally fit atop the removable drawer, within the confines of the base compartment. Receptacles within either the base compartment or the drawer may contain a pharmaceutical formulation comprising insulin. The medical case allows the patient to access needed medical and nutritional supplies and access equipment necessary to monitor and/or control his/her glucose level.

Abstract: A system for use in an orthopaedic surgical procedure including a container for orthopaedic surgical instruments. The container includes a first shell, and a second shell configured to be coupled to the first shell to define a chamber therein. The second shell is configured to be coupled to the first shell in a plurality of orientations including a first orientation in which fluid is permitted to advance into and out of the chamber, and a second orientation in fluid is prevented from advancing into and out of the chamber.

Abstract: A rack for surgical sponge counter bags that facilitates sponge counting, comprising a spindle and a plurality of rotatable support members mounted for rotation about the spindle, each support member carrying one or more mechanical devices that are constructed and adapted to grasp a sponge counter bag.

Abstract: A cancellation feature (2203) for a pharmaceutical waste disposal assembly (10) having a first surface (2201) and a second surface (2202) can include a first cancellation member (2204) that is secured to the first surface (2204) and a second cancellation member (2205) that is secured to the second surface (2205). The second cancellation member (2205) automatically moves from a pre-engaged configuration that allows engagement with the first cancellation member (2204) to a post-engaged configuration that inhibits engagement with the first cancellation member (2204). The automatic movement occurs after engagement and/or during disengagement between the second cancellation member (2205) and the first cancellation member (2204). The first surface (2201) can form a portion of a receiver that receives pharmaceutical waste, and the second surface (2202) can form a portion of a receiver retainer that retains the receiver.

Abstract: A substantially rigid defibrillator carrying case having a hinged side, a latch disposed on a latch side opposite the hinged side, and a handle disposed on a handle side disposed between the hinged side and the latch side. The carrying case is constructed without protrusions and with a rigid handle, which combine to allow easy removal and deployment of the contents from a vehicle storage location to a cardiac arrest patient. The carrying case is further constructed for greater ease of use during rescue, greater ro-bustness, and for ease of maintenance.

Abstract: Disclosed are various embodiments for holding and organizing surgical instruments in a surgical environment. In one embodiment, a surgical instrument holder comprises an elongated body portion including a plurality of slots. Each of the slots may be configured so as to retain a surgical instrument in a fixed position. The elongated body portion may have a base surface configured to contact a table surface.

Abstract: An apparatus to support various surgical instruments is disclosed. The apparatus may include numerous chambers that may be used to separate different instruments. The chambers may have grooves that are used to support the instruments, and the height of the apparatus from the supporting surface may be comparable to the measurements of the instruments to provide a securing surface.

Abstract: The purpose of the present invention is to facilitate the extraction of plate-shaped biosensors stored in a container body. More specifically, a body for storing biosensors is provided, the body including: a tube-shaped storage container body having an open upper face; a lid body for covering the upper face opening of the storage container body so that the lid can open and close the upper face opening; and plate-shaped biosensors stored within the tube-shaped container body. The biosensors are each provided with a measurement section disposed at one end thereof; a connection terminal section disposed at the other end thereof; and a connection section disposed between the one end and the other end and electrically connecting the measurement section and the connection terminal section. The biosensors each have a protrusion disposed at an end thereof in the longitudinal direction thereof.

Abstract: This application describes example antimicrobial compositions that may be used alone or in combination with catheters and catheter insertion sites. According to another aspect, the application describes catheters which may employ one or more protection devices, such as cleaning caps, protective caps or both.

Abstract: A novel container for storing medical guidewires in liquid is disclosed herein. The container comprises a substantially rectangular basin where the guidewire coils are separated horizontally into individual bays. Specific tabs and dividers hold the coils in place and keep the wires untangled. The horizontal placement of the wires enables a clinician to instantly differentiate between wires, select the right coil without spending time in untangling wires and allows storing of the wires is relatively small amount of storing liquid.

Abstract: An adjustable surgical instrument stringer, tray system, and method of sterilization comprising, in general, a one or more axis adjustable stringer to be inserted into the finger rings or ring handles of the surgical instruments to sequentially group the surgical instruments, a surgical instrument tray and lid configured with a pattern of sterilization apertures, the lid having two or more recessed valleys configured to receive the stringer of ringed surgical instruments and releasably hold the surgical instrument therein.

Abstract: A surgical instrument securing device is provided for holding medical instruments. The surgical instrument securing device may be formed from a silicone, rubber, or other polymer based base and may be elastomeric. Slots in the base may define one or more substantially arcuate, circular, elliptical, or other geometrically shaped spaces within the base which open towards at least one side of the base, wherein one or more surgical instruments may be secured by inserting a portion of the instrument into one of the slots. A method for securing surgical instruments is also provided wherein surgical instruments are secured by inserting a portion of the instruments into the slots within the silicone or other polymer based base.

Abstract: A lid covering an interior of a medical waste receptacle base. The lid includes an intermediate waste repository connected to the cover. The repository is moveable between a holding position adapted for holding waste segregated from the receptacle base interior, and a dumping position adapted for biasing waste by gravity into the receptacle base interior.

Abstract: A storage system for storing used surgical towels, sponges or other medical waste materials includes a rear panel having an upper portion and a lower portion formed from a flexible sheet material. The upper portion of the rear panel has a coupling mechanism for coupling the device to a sterile structure of a surgical room. In certain embodiments, the rear panel may have a weakened partition area for separating the lower portion from the upper portion. A compartment assembly is formed by two or more flexible compartments provided on the lower portion of the rear panel. Each compartment may be liquid impervious and have an upper opening for introducing materials into the compartment. Each compartment has a forward wall that is at least partially transparent so that the contents of the compartment are observable. All components of the storage device may be sterile for use in a sterile environment. In certain embodiments, a storage system may be provided by coupling at least two storage devices together.

Abstract: A pharmaceutical waste disposal assembly (1810) for disposing of sharps and one or more of fluid pharmaceutical waste and solid pharmaceutical waste includes a receiver assembly (1851) having a sharps receiver (1815), a waste receiver (1812), and a receiver retainer (1816). The sharps receiver (1815) receives sharps. The sharps receiver (1815) includes a sharps receiver body (1823) that defines a sharps region (1827C). The waste receiver (1812) receives one of fluid pharmaceutical waste and solid pharmaceutical waste. The waste receiver (1812) includes a waste receiver body (1819) that defines a waste region (1827A) that is independent of the sharps region (1827C). The receiver retainer (1816) receives the sharps receiver (1815) and the waste receiver (1812). The sharps receiver body (1823) and the waste receiver body (1819) are positioned substantially adjacent to one another within the receiver retainer (1816).

Abstract: A handling system for use in the manufacture of syringe barrels includes a tray having an array of apertures with a tubular upstand around each aperture, each upstand at the upper end thereof defining a support surface for a syringe barrel. Each syringe barrel comprises a cylindrical part and an enlargement at or adjacent the rear end of the barrel and carries at its forward end a safe needle device or a needle shield of a greater diameter than the syringe barrel. At least one of the enlargement of the syringe barrel or the support surface has a profile tapering or rounded inwardly in the downward direction so that when the tray is supported generally horizontally and a syringe barrel is lowered into an upstand, the syringe barrel is centred by co-operation between the enlargement and the support surface. The enlargement may be a flange at the rear end of the syringe barrel or could be a further component fitted to the barrel.

Abstract: A surgical apparatus for use by a surgeon can include a tray and a plurality of surgical instruments. The tray can have a plurality of structures located on an upper side of the tray for receiving the plurality of surgical instruments. The tray can receive a separate control unit. The tray can also have a fluid reservoir receiver for receiving a bottle or container of fluid, such as balanced salt solution. The fluid reservoir receiver can include one or more features, including, a spike, an air vent, and a light. A separate container can be used to place the bottle or container of fluid into the fluid reservoir receiver on the tray. This separate container can include a collapsible section.

Abstract: A sheath remover device is of elongate tubular form having a sheath capture region at one end and a passage along which a captured sheath may pass from the capture region. A plurality of latching fingers, each with an internally directed latch, are equi-spaced in the capture region. Two further inwardly directed latches are on the cut out regions. The sheath remover is designed so that, a sheath already disposed in the sheath capture region is pushed along the passage away from the sheath capture region when the remover is offered up to and engages the subsequent sheath. The spacing of the latches and is such that the earlier sheath is not released from latches until the latches have securely engaged in the subsequent sheath, thereby providing an indication of secure engagement of the subsequent sheath. The sheath remover may also be used as a cap and/or a cocking rod.

Abstract: An apparatus includes a medicament container and a package. The medicament container includes a wall configured to define a medicament reservoir. The wall includes a protrusion configured to propagate a deformation of the wall when an external force is applied to the protrusion to reduce a volume of the medicament reservoir. The package includes a blister portion and a foil portion and defines a cavity therebetween. The blister portion is configured to cover the medicament reservoir when the medicament container is disposed within the cavity.

Abstract: A pack of oral care items that allows for simultaneous opening and easy access to the items contained in the pack. The pack of oral care items includes two or more flexible packages. The flexible packages may be arranged in parallel. One flexible package may be an inner package that is located substantially within another flexible package that forms an outer package. The inner package may include an integral burst pouch configured to release a liquid into an interior space of the outer package while keeping the interior space of the inner package dry. Each flexible package includes a frangible region located at or adjacent a top portion and at least one oral care item is disposed within an interior space of each flexible package.

Abstract: A package is provided to include first and second sheets being releasably sealed together in a manner to define multiple compartments, each having one or more medical implements. A perimeter sealed region can have a seal width greater than an intermediate sealed region. A longitudinal intermediate sealed region and a transverse intermediate sealed region can be arranged within the perimeter sealed region. Formation of the perimeter sealed region along first and second ends of the package can be subsequent to the perimeter sealed region along third and fourth ends of the package. Before the formation, compartments having an opening facing the first end can receive medical implements, and compartments having an opening facing the second end can receive medical implements. The medical implements can remain uncovered by individual pouches when inserted into the respective compartments, thereby reducing manufacturing costs and environmental wastes.

Abstract: Packaged systems for implanting a marker in a patient and methods for manufacturing and using such systems. In one embodiment, a packaged system comprises an introducer having a cannula and a stylet configured to be received in the cannula, a marker in the cannula, and a package having a sterile compartment. The marker can have a casing configured to be implanted in a patient and a resonating circuit in the casing. The resonating circuit can comprise a coil configured to wirelessly transmit a target signal in response to a wirelessly transmitted excitation signal. The introducer is contained within the sterile compartment. In another embodiment, the marker is not loaded in the introducer within the compartment of the package.

Abstract: A sealed foil pouch has a textured opening flange and includes first and second foil sheets having opposing inner surfaces joined together by a seal for defining a sealed area of the pouch located inside the seal and an unsealed area of the pouch located outside the seal. The sealed pouch includes a textured opening flange located adjacent an edge of the pouch for peeling the first and second foil sheets away from one another for breaking the seal and opening the sealed pouch. The textured opening flange is located within the unsealed area of the pouch and includes at least one roughened surface formed on at least one of the first and second sheets. A leg of the seal passes through the textured opening flange. The roughened surface makes it easier to break the leg of the seal for pulling the sheets apart.

Abstract: A prosthetic assembly A prosthetic assembly (10) comprising: a body portion (12); first and second flanges (14, 16) provided on a rim (18) of the body portion; the first and second flanges being provided with first and second openings (20, 22) respectively; and a bridging member (24) connectable to the first and second flanges such that the member spans between the first and second flanges, the member being provided with a third opening (26); wherein the first, second and third openings are suitable for receiving first, second and third bone attachment members (28, 30, 32) respectively.

Abstract: A sterilization container having surgical implement/implant holders with flexible edges. Each holder is in the form of a pair of brackets which are positioned tightly on either side of a flexible wall for cooperatively forming a composite holder with an upwardly opening recess. The flexible wall of each holder extends beyond edges of its respective pair of brackets for forming the flexible edges which are used to support the surgical implements/implants. Outwardly turned feet on the bottom of each of the pair of brackets are placed through holes on a base wall of the sterilization container for securing each holder to the container.

Abstract: Devices and methods are disclosed for protecting individuals from the sharp ends of medical objects following use on a patient. Such sharp objects include hypodermic needles, scalpel blades, cannulae, trocars, and the like. The invention utilizes a disposable protective cover for the used sharp. The protective cover is designed to surround and embed the sharp in a permanent cover that is blunt and will not permit further puncture or cutting with the sharp. In an embodiment, the protective cover also absorbs any fluids on or in the used sharp and prevents any fluids from escaping the protective cover. The sharp cover is configured to irreversibly lock, once closed. A refillable or replaceable dispenser dispenses the protective covers at points of use. A disposable receptacle receives the used sharp embedded in the protective cover. When the receptacle is full, the entire receptacle may be discarded in a medical waste container.

Abstract: Inductively coupled shelving units and storage containers with integrated primary coils, as well as inductively coupled systems for storing and charging tools, are provided. Power is inductively coupled from a primary coil to a device containing a secondary coil. Primary coils may be integrated into a shelving unit to charge devices stored on the shelving unit. Primary coils may similarly be integrated into a storage container. Inductively coupled shelving units may also be configured to receive and hold an inductively coupled storage container such as a toolbox. An integrated secondary coil in the toolbox receives power inductively coupled from a primary coil in a shelving unit. Integrated primary coils in the toolbox then inductively couple the received power to secondary coils in individual devices. Integrated primary coils may provide varying amounts of power.

Abstract: The present invention is directed to a laparoscopic device insertion cannula (“LDIC”). The LDIC can be configured to store a surgical implant and can be formed from a hollow cylindrically shaped tube including a tapered closed tip at a distal end and a cap at a proximal end. The hollow tube can also include an opening adjacent the distal end. The opening can be covered, for example, by a flexible window. The flexible window can include a slit from which the surgical implant can be extracted from the LDIC. The surgical implant can be, for example, a gastric band.

Abstract: A single package infusion set is provided, including one or more of the following inserters: pushbutton-type, squeeze-type, contact-type, skin pinching-type, folding retraction-type, or multistage-type inserter having at least one reusable stage. The infusion set further includes adhesion means with user-selectable degrees of adhesion strength, self-sealing tube connection means, a lens feature to view, a site beneath the set, exemplary tube management and connection elements, insulin supply, adhesion concealment means, finger loops on the inserter and site preparation wipes or sprays, optionally provided as part of the inserter. The system further includes a package which may hold a number of easily released sets, retrievable by an inserter, an exemplary insertion needle handle and shroud, an exemplary squeeze-type latch between an upper portion and a lower portion of the set, and/or a tool removable upper portion of the set.

Abstract: This invention protects the processes and technologies used to produce kitting foam inserts. The manufactured inserts are in the form of foam silhouettes with a thin hard plastic backing. The process is unique in that it utilizes software and automations that were previously unknown in the kitting industry. The hard plastic backed foam inserts will retain the positions of items within the kit and allow, at a glance, identification of missing or displaced items and tools. The foam inserts also provide for rapid restocking of reusable assembly kits. Pocket marks can incorporate human and/or machine-readable symbols into the foam inserts. This patent is unique with respects to the referenced U.S. Pat. No. 7,410,053 B2 in that this invention describes in detail the manufacturing process for producing foam kitting inserts to be used for organizing tool and assembly kits.

Abstract: A surgical pack includes a platform having a plurality of recesses configured to function as a surgical tray. A plurality of surgical instruments are contained in a corresponding recess of the platform. The recess may have the shape of the surgical instrument that it is designed to receive. The recess may also include safety mechanisms to protect the tips of certain instruments and to lower the risk of injury caused by them. A packaging or covering holds the platform and the plurality of surgical instruments in a substantially sterile condition.

Abstract: A portable surgical tray unit can include a portable surgical tray for housing a processing unit, and that includes an opening extending entirely therethrough. The portable surgical tray unit can also include a plurality of instruments connected to the portable surgical tray and operably coupled to the processing unit, and a user input device positioned on at least one of the instruments. The user input device can be operably coupled to the processing unit and can be configured to receive a user input for controlling an operating parameter of one or more of the instruments. The processing unit can be configured to receive user input through the user input device and transmit an operating command to the one or more instruments. The portable surgical tray and the plurality of instruments can be sterilized and prepackaged in a single package.

Abstract: A surgical kit comprises two percutaneous instruments each having an elongate shaft with a distal end and a proximal end connected to a handle; at least two end effectors attachable and detachable to the distal ends of the percutaneous instruments; a laparoscopic loader adapted to receive the end effectors; a trocar; and a laparoscopic surgical stapler. The surgical kit may further comprise laparoscopic energy based clamping and coagulating device and/or a laparoscopic suture device. Optionally, the surgical kit may further comprised a third percutaneous instrument having an elongate shaft with a distal end and a proximal end connected to a handle, and at least three end effectors attachable and detachable to the distal ends of the percutaneous instruments. The surgical kit may further comprise a magnetic camera and/or a magnetic external control unit adapted to anchor a magnetic camera. The components of the surgical kit may be contained in a sterile sealed package.

Abstract: Devices and methods are disclosed for protecting individuals from the sharp ends of medical objects following use on a patient. Such sharp objects include hypodermic needles, scalpel blades, cannulae, trocars, and the like. The invention utilizes a disposable protective cover for the used sharp. The protective cover is designed to surround and embed the sharp in a permanent cover that is blunt and will not permit further puncture or cutting with the sharp. In an embodiment, the protective cover also absorbs any fluids on or in the used sharp and prevents any fluids from escaping the protective cover. The sharp cover is configured to irreversibly lock, once closed. A refillable or replaceable dispenser dispenses the protective covers at points of use. A disposable receptacle receives the used sharp embedded in the protective cover. When the receptacle is full, the entire receptacle may be discarded in a medical waste container.