Abstract: A medical device assembly is disclosed, comprising a medical device, preferably having a hydrophilic surface coating, and a package accommodating said medical device. The package if formed of two sheets of foil material, a first foil of which has been deep drawn into a trough shape, the package further comprising a resealable opening arranged within the bounds of the second foil. The medical device may e.g. be a urinary catheter.

Abstract: A catheter assembly is disclosed, comprising a catheter and an elongate package accommodating said catheter in a closed condition. The package is provided with an insert opening arranged to releasably receive an end of the elongate package in the closed condition, thereby temporarily retaining said closed package in a folded disposition in which also the catheter is folded.

Abstract: A catheter assembly includes a catheter, preferably having a hydrophilic surface coating; and a package accommodating said catheter. The package preferably also accommodates a wetting fluid. The package includes a first and a second sheet material connected around the edges; a perforation line extending along a non-closed loop in one of said sheet materials, which defines a flap opening; a third sheet material connected by means of an adhesive over said flap opening. The third sheet material with a margin covers the entire flap opening. The adhesive is adapted to maintain a sterile closure of the package before use, and to be resealable after use. The third sheet material forms a tab not provided with adhesive and the tab provides a grip portion for peel opening of the package.

Abstract: A packaged incontinence treatment device includes a catheter and a package. The catheter has a distal tubular portion that is connected to a sheath with a portion of the sheath rolled to provide a proximal collar. The package encloses the catheter and includes a lower portion coupled to an upper portion by a hinge plate. The hinge plate is adapted to allow the upper portion to pivot away from the lower portion to provide an opened package configuration and to allow the upper portion to pivot toward the lower portion to provide a closed package configuration. The package has a retainer protrusion extending from an interior surface of the package that is engaged with the proximal collar of the catheter and retains the proximal collar in the lower portion of the package.

Abstract: A syringe assembly including a plunger rod separate and detached from a syringe barrel and a packaging member, the plunger rod having a sealing member and the packaging member having a first compartment and a second compartment is disclosed. With the syringe barrel received within the first compartment and the plunger rod received within the second compartment, the sealing member of the plunger rod seals the syringe barrel and the plunger rod within the packaging member. In this manner, the syringe assembly is placed in the packaging member in a manner that allows for reduced storage space of the syringe assembly. In one embodiment, the syringe assembly includes an engagement portion connected to the plunger rod and a stopper slidably disposed within the interior of the syringe barrel, the engagement portion operable to secure the plunger rod to the stopper.

Abstract: A protective tubing assembly having male and female connectors integrally formed along its exterior surface and an asymmetrical cross-section with additional wall thickness in the non-connector cross section regions is provided by the present invention. Cooperating, substantially flat exterior bearing surfaces may also be formed along the exterior surface of the tubing. The tubing can be wound into coiled alignment with the male and female connectors securing adjacent coils together, and the additional wall thickness regions in the asymmetrical cross-sectional reducing unwanted twisting of the tubing that would otherwise lead to individual coils rising from their original, substantially planar coiled alignment. An extrusion manufacturing process with special inner and outer dies is also provided.

Abstract: A medicament delivery device includes a housing, a medicament container disposed within the housing, an activation mechanism, a cover and an electronic circuit system. The activation mechanism includes an energy storage member configured to produce a force to deliver the dose of a medicament and/or vaccine. The cover is configured to receive at least a portion of the housing. The electronic circuit system is coupled to the housing such that a protrusion of the cover electrically isolates a battery from a portion of the electronic circuit system when the portion of the housing is received by the cover. The electronic circuit system is configured to be electrically coupled to the battery and to produce a recorded speech output when the portion of the housing is at least partially removed from the cover. The electronic circuit system configured to produce a signal when the activation mechanism is actuated.

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: The invention includes a device having a chamber within a syringe. A fluid passageway extends through a syringe piston. A valve is associated with the passageway controlling fluid passage through the piston. The invention includes a piercing structure having a head segment and a body portion, with a channel through the body portion and through at least one surface of the head without passing through the tip. In another aspect the invention encompasses a method of preparing an agent for administration to an individual. A first component is provided within a syringe and a second component is provided within a vial. A closed valve is associated with a fluid passageway between the vial and the syringe barrel through a piston. Valve repositioning allows fluid passage and sliding of the piston joins the first and second components. Repeated sliding of the piston mixes the components to produce the medication agent.

Abstract: A stand for use with a syringe is structured to engage a portion of the syringe in order to maintain the syringe in an upright position. The stand may include an aperture structured to engage the nozzle or the plunger of the syringe. Another embodiment of the stand may include a protrusion structured to engage the proximal end of the syringe, or a clip structured to engage a handle of the syringe. The stand may include a package portion having compartments for holding various components, such as components of a bone cement preparation kit. The proximal and distal portions of the barrel of the syringe may be separable to provide an opening into the barrel through which an injectable material may be inserted. The plunger of the syringe may also include a plunger rod removably affixed to the plunger tip.

Abstract: Packaging for a catheter includes coiled tubing for receiving the catheter and a mounting card coupled to the coiled tubing. The windings of the coiled tubing are welded together to maintain the coiled configuration. The mounting card includes an integral support flap for reducing the risk of damage during catheter insertion and removal, an integral luer retainer for securing a catheter luer, and one or more integral tabs for attaching catheter accessories to the packaging. The integral support flap creates a contact zone which discourages grasping the packaging at a location that can potentially damage an object passing through the packaging, such as a balloon and/or stent. The integral luer retainer is configured to selectively alternate between a configuration which secures the catheter luer and configuration which allows releases the luer for easy insertion and removal of the catheter.

Abstract: A syringe including a front end and a rear end. A front portion of the syringe having an axially extending hollow needle that projects from the front end. The rear end of the needle is in fluid communication with a space that extends substantially to the rear end of the syringe. A plunger extends axially and is movable to and fro in the space and is designed such that, when drawn out, it sucks liquid through the needle and, when pressed in, discharges liquid through the needle. A radially projecting flange element in the front portion of the syringe is designed in such a way that it can be gripped between the thumb and middle finger of a user's hand. The syringe is dimensioned so as to permit injection using the index finger of the same hand. A capsule device for at least partially accommodating a syringe. A syringe device.

Abstract: A pre-packaged medical device includes a tray supporting a medical device such as a blood collection set including a needle assembly and a tube holder. The tray defines a first contoured portion supporting at least a portion of the needle assembly and a second contoured portion supporting the tube holder. The tray may have a tray body with a plurality of posts upstanding from a bottom wall in the first contoured portion for engaging the needle assembly. The posts may be positioned to maintain the needle assembly in a defined orientation while preventing the inadvertent actuation of the needle assembly, which may include a spring-driven safety shield. The configuration of the pre-packaged medical device allows sequential removal of the blood collection set, typically in the order of intended use including first removal of a needle assembly, second removal of tubing, and third removal of the tube holder.

Abstract: Medical device packaging, medical device packaging assemblies, and methods for preparing and packaging medical devices. An example medical device packaging assembly may include a pouch having a pocket formed therein. A carrier tube may be disposed in the pocket. The carrier tube may have a plurality of apertures formed therein. A medical device may be disposed within the carrier tube.

Abstract: A medical device packaging comprising a connector coupled to a longitudinal element having a lumen sized and shaped to receive an shaft of a medical device extending distally from a hub of the elongate member. The connector including a first branch having a lumen open to the lumen in the elongate member and a second branch having lumen open to the lumen in the first branch. A proximal end of the first branch being configured to mate with a distal end of a housing of the medical device to be received in the packaging. The hub of the medical device including laterally extending wings having opposing contours. The medical device including a strain relief member coupled at a distal end of the hub of the medical device.

Abstract: The present invention relates to a package comprising a container defining a compartment for containing a liquid and at least partly a medical device. The compartment extends in a longitudinal direction from a bottom of the container towards an opening of the container, wherein a first section of the compartment has a cross-sectional area which is smaller than a cross-sectional area of a second section of the compartment, and where the first section is arranged between the opening and the second section. As the cross-sectional area of the first section is smaller than the cross-sectional area of the second section the first section will function as a stop for the liquid in case the container is placed in a horizontal orientation.

Abstract: A system includes a medicament delivery device and a container configured to receive at least a portion of the medicament delivery device. The medicament delivery device includes an actuator and a first electronic circuit system. The actuator is configured to initiate delivery of a medicament into a body when the actuator is moved from a first position to a second position. The first electronic circuit system is configured to output a first electronic signal when the actuator is moved from the first position to the second position. The container includes a second electronic circuit system configured to receive the first electronic signal. The second electronic circuit system is configured to output a second electronic signal associated with the first electronic signal.

Abstract: A catheter holder which is compact and which can be relatively easily released while holding the unhoused portion of the catheter stably includes: an attachment portion for receiving or being attached to a portion of a holding tube housing a portion of the catheter, and a plurality of hold portions integral with the attachment portion and holding an unhoused portion of the catheter, which is exposed outside the holder tube.

Abstract: This invention relates generally to systems for imporving the safety in medication use. Specifically, the invention relates to the use of matching drug name voice templates as a threshold mechanism for unlocking a medication container.

Abstract: A vapor hydrated packaged catheter assembly and method of manufacturing and distributing same includes a gas impermeable package housing a catheter within a catheter-receiving cavity. The catheter assembly has a hydrophilic coating applied to at least a portion of the outer surface of a catheter tube or shaft which may be surrounded by a sleeve to provide a no-touch, sure grip feature. The catheter assembly is disposed within the catheter receiving cavity of the package together with a limited amount of a vapor donating liquid provided as a source of vapor to activate the hydrophilic coating. The amount of vapor donating liquid is less than the amount that would otherwise be sufficient to cause a spill hazard. It may be loose liquid as a desired percentage of the volume of a tube-receiving portion of the catheter receiving cavity of the package, or it may be contained in a liquid sequestering element.

Abstract: A package is described having two blanks of a sheet material joined along edges to form one or more enclosed compartments to retain a urinary catheter. The joined edges provide at least one peeling zone permitting separation of two foil walls. A gripping means is provided to allow a firm grip relative to the peeling zone.

Abstract: Package for a catheter, with a catheter having catheter tube with a distal end and a proximal end, the proximal end being provided with a catheter connector. A main body is provided for holding the catheter, and a cap for closing off the main body. A gel container is positioned inside the main body, the gel container being provided with a cavity for holding an amount of a lubricating agent. The gel container includes a first opening at a distal end thereof, and a second opening at a proximal end thereof.

Abstract: A medical waste disposal apparatus for receiving and retaining waste articles, such as catheter fittings, and the like, for controlled and facilitated handling and disposal of such waste articles, during and following the performance of treatment procedures on a patient by a practitioner. The waste disposal apparatus includes a first retaining member, mounted on a base panel, for receiving and retaining a waste article placed there by a practitioner during a treatment procedure, and further includes at least one side panel, for covering the waste article, after placement of the waste article on the first retaining member. Alternative configurations of retaining members are provided.

Abstract: An apparatus includes a container defining an internal region configured to contain multiple medicament delivery devices, such as, for example, pen injectors, auto-injectors, inhalers or the like. The container includes an electronic circuit system configured to output a first electronic output associated with a first medicament delivery device contained within the internal region when the first medicament delivery device is removed from the internal region of the container. The electronic circuit system is further configured to output a second electronic output associated with a second medicament delivery device contained within the internal region when the second medicament delivery device is removed from the internal region of the container. The second electronic output is different than the first electronic output. At least one of the first electronic output or the second electronic output is associated with a use instruction.

Abstract: A catheter assembly (110, 210) comprising a catheter (130, 230) and a receptacle (120, 220) is disclosed. The receptacle is arranged to accommodate at least part of said catheter and having at least one opening (123) for withdrawal of said catheter. Further, the receptacle is provided with an antimicrobial compound (301) at least in the vicinity of the opening and at least on the outer surface of the receptacle, said antimicrobial compound inhibiting microbes from being transferred to said catheter while being withdrawn through said at least one opening.

Abstract: Medical device packaging, medical device packaging assemblies, and methods for preparing and packaging medical devices. An example medical device packaging assembly may include a pouch having a pocket formed therein. A carrier tube may be disposed in the pocket. The carrier tube may have a plurality of apertures formed therein. A medical device may be disposed within the carrier tube.

Abstract: A medical implement dispensing and disposal system. The medical implement dispensing and disposal system comprises a container having an open end with a dispensing chamber and a disposal chamber defined within the container. A cover is configured to substantially close the open end of the container. The cover defines a disposal opening in communication with the disposal chamber. A dispensing opening is defined in either the container or cover and in communication with the dispensing chamber. A biasing assembly is positioned in the dispensing chamber and configured to provide a biasing force toward the dispensing opening.

Abstract: A medical device holder is comprised of a flexible elongated sheet member, and includes a holding portion configured to hold a three-dimensionally configured part connected of the device. The holding portion is configured to bend back on itself to cover the three-dimensionally configured part. A slit is provided in the sheet member to allow insertion of the distal end portion of the holding portion so that the state in which the holding portion covers the three-dimensionally configured part connected can be maintained. The distal end portion of the holding portion is folded toward the opposite direction from the direction to pull out when retrieving the catheter from the sheet member.

Abstract: A tray stack (100) for accommodating a catheter assembly (1400) and medical devices (1401,1402,1403,1404,1409,1410, 1411,1412,1413) corresponding to catheter use includes a first tray (101) and second tray (102). Each tray (101,102) includes a tray opening, a base member (205,206), and sidewalls (203,204). When placed atop each other, they first tray (101) and second tray (102) form a tray stack (100). When unstacked and placed in a side-by-side, single layer catheter tray assembly (200), implements disposed therein can be arranged in a predetermined sequence corresponding to an order of use during a catheterization procedure. Mechanical couplings (300) can be included to permit the trays to translate with respect to each other. Retention mechanisms (710-713) can be included to hold the trays together.

Abstract: A syringe device having a syringe barrel and a syringe piston having a container housing. At least a portion of the container housing is insertable within an internal chamber of the syringe barrel. A fluid passageway extends from the container housing through a piston stem. A method of protecting a syringe handler including providing the components of a syringe device and encasing the components in a protective film. The protective film is loose to allow manipulation of the syringe components relative to one another without opening or puncturing the film. Protective syringe device packaging that includes a laminate film of material sealed to encase the components of a syringe device containing a potentially harmful agent.

Abstract: A catheter product package and method of forming same in which the package comprises a sheet material wrapped about the catheter product to form a package for the catheter product. The catheter product extends generally longitudinally within the package, and the sheet material extends from a point beyond the proximal end to a point beyond the distal end of the catheter product. The sheet material of the package is wrapped about the catheter product in a manner defining confronting proximal end edges, confronting distal end edges, and confronting side edges. The confronting proximal end edges, distal end edges and side edges of the sheet material are joined by a seal after the sheet material is wrapped about the catheter product to define a sealed cavity. The sheet material has a tear strip affixed to it which causes the sheet material to tear along the tear strip to thereby cause the package to open along an intended opening line.

Abstract: A catheter assembly is disclosed comprising a catheter and a receptacle enclosing said catheter. The receptacle has a first part and a second part, which parts are foldable over each other. Further, at least one sticky adhesive area is arranged on the surface of one of the parts of the receptacle in such a way that the sticky adhesive area is covered by the other part when the receptacle is in a folded disposition, and exposed to the environment when the receptacle is in an unfolded disposition.

Abstract: A vapor hydrated packaged catheter assembly includes a gas impermeable package housing a catheter within a catheter-receiving cavity. The catheter assembly has a hydrophilic coating on at least a portion of the outer surface of a catheter tube which may be surrounded by a sleeve. The catheter assembly is disposed within the catheter receiving cavity of the package with a vapor donating liquid provided as a source of vapor to activate the hydrophilic coating. The amount of vapor donating liquid is less than the amount that would otherwise be sufficient to cause a spill hazard. The catheter assembly is ready to use due to exposure of the hydrophilic coating to a vapor produced by the vapor donating liquid.

Abstract: The invention provides a device for securing an invasive medical implementation, such as a catheter, to a patient. The device generally combines an adherent surface that attaches the device to the skin and a flexible clasping means to grasp the catheter and reversibly secure it to the device.

Abstract: A catheter assembly allowing for non-contaminated insertion of the catheter into the urinary canal. The catheter assembly includes a urinary catheter, a catheter package and a sealing member. The urinary catheter defines a conduit and has a proximal end adapted for insertion into the urinary canal and an opposite distal end. The catheter package has a hose with a cavity for accommodation of the catheter, and a catheter outlet adapted to dismantle the proximal end of the catheter from the catheter package. The sealing member is adapted to provide a substantially liquid-tight seal between the catheter package and the urinary catheter while the catheter is being dismantled.

Abstract: An assembly comprising a packaging device (20) and an intraocular lens injector (10) comprising a body (11) that contains an intraocular lens, said packaging device (20) being for receiving and storing said injector (10) prior to use, said packaging device (20) being made of a material that is waterproof, and being filled with a storage solution for maintaining at least the body (11) of said injector (10) and the intraocular lens in total immersion throughout the duration of storage, said packaging device (20) comprising a substantially rigid container (21, 22) and an opening (25) for enabling said injector (10) to be installed and removed, said container (21, 22) including at least one internal shoulder (26, 27) co-operating with a portion of the injector (10) to center and maintain its lens ejector end (14) away from the walls of said container (21, 22).

Abstract: A package for elongate medical devices such as guide wires or catheters. The package includes an elongate tube wound into a spiral coil configuration and a first clip overmolded onto the tube such that the first clip surrounds the tube at adjacent sections of the tube to maintain the coil configuration.

Abstract: A package including an intermittent urinary catheter and a protective sleeve is provided. The protective sleeve is adapted to cover the surface of the catheter prior to use, thereby preventing contamination of the surface. The protective sleeve is compressed in a storage-position, and in a use-position it is extended to cover most of the insertable length of the catheter. In the compressed state, the urinary catheter may be wetted if the catheter is provided with a hydrophilic coating. The protective sleeve may be made of flexible material, which may be folded or pre-folded into a concertina-like configuration. A package which includes an intermittent urinary catheter with a protective sleeve is provided. An assembly, which includes a package with an intermittent urinary catheter, and a compartment containing a fluid medium, is provided. Finally, a method for wetting an intermittent urinary catheter including a protective sleeve is provided.

Abstract: A pharmaceutical pig is used to transport a syringe containing a liquid radiopharmaceutical from a radiopharmacy to a medical facility for administration to a patient. The pharmaceutical pig includes an elongate polymer cap that is removably attached to an elongate polymer base. The elongate polymer cap includes a cap shell that completely encloses a cap shielding element and the elongate polymer base includes a base shell that completely encloses a base shielding element. Preferably the polymer utilized for the cap shell and the base shell is polycarbonate resin, e.g., LEXAN®. An inner liner is not utilized and the cap shielding element and the base shielding element, which are preferably, but not necessarily, made of lead, are completely sealed and unexposed.

Abstract: A pharmaceutical pig is used to transport a syringe containing a liquid radiopharmaceutical from a radiopharmacy to a medical facility for administration to a patient. The pharmaceutical pig includes an elongate polymer cap that is removably attached to an elongate polymer base. The elongate polymer cap includes a cap shell that completely encloses a cap shielding element and the elongate polymer base includes a base shell that completely encloses a base shielding element. Preferably the polymer utilized for the cap shell and the base shell is polycarbonate resin, e.g., LEXAN®. An inner liner is not utilized and the cap shielding element and the base shielding element, which are preferably, but not necessarily, made of lead, are completely sealed and unexposed.

Abstract: A reloadable medicine injector and methods are described in which a barrel with a receiving cavity is adapted to slidably receive a syringe subassembly for axial movement therein. Upon removal of a safety and release of a syringe driver, the syringe driver moves forward and injects the syringe needle. A plurality of penetration controls are shown for controlling injection needle penetration depth. The penetration controls have an abutment and various lengths to provide different needle penetration depth positions. In one form of penetration control a sleeve is used against which the syringe or related parts contact. In another form the front return spring is used as a penetration control. A cushioning ring may be used to reduce syringe breakage. A load distribution and guide ring may be used to distribute loading applied to the syringe and help guide the moving syringe.

Abstract: A catheter assembly is disclosed comprising a catheter, preferably having a hydrophilic surface coating; and a package accommodating said catheter. The package preferably also accommodates a wetting fluid. The package comprises: a first and a second sheet material connected around the edges; a perforation line extending along a non-closed loop in one of said sheet materials, said perforation line defining a flap opening; a third sheet material connected by means of an adhesive over said flap opening, wherein said third sheet material with a margin covers the entire flap opening. The adhesive is adapted to maintain a sterile closure of the package before use, and to be resealable after use. Further, the third sheet material forms a tab not provided with adhesive, said tab providing a grip portion for peel opening of the package.

Abstract: An assembly including a component of a surgical instrument, such as an endoscopic or laparoscopic instrument. The assembly may comprise a package; a surgical instrument component within the package; and a power source within the package. The power source may be configured to be placed in electrical communication with the surgical instrument component. The assembly may also comprise an auxiliary power source within the package and a circuit element, where the circuit element is in electrical communication with the power source and the auxiliary power source.

Abstract: A retainer for maintaining a tubular sheath used to store a catheter guide wire in a coiled configuration includes a body having a bottom defining a plurality of substantially parallel channels. Each channel is designed to closely receive a coil of the tubular sheath. A loop is affixed to and extends adjacently above the body and defines an aperture therethrough for receiving and guiding the catheter guide wire after removal of the guide wire from the tubular sheath.

Abstract: A vapor hydrated packaged catheter assembly and method of manufacturing and distributing same includes a gas impermeable package housing a catheter within a catheter-receiving cavity. The catheter assembly has a hydrophilic coating applied to at least a portion of the outer surface of a catheter tube or shaft which may be surrounded by a sleeve to provide a no-touch, sure grip feature. The catheter assembly is disposed within the catheter receiving cavity of the package together with a limited amount of a vapor donating liquid provided as a source of vapor to activate the hydrophilic coating. The amount of vapor donating liquid is less than the amount that would otherwise be sufficient to cause a spill hazard. It may be loose liquid as a desired percentage of the volume of a tube-receiving portion of the catheter receiving cavity of the package, or it may be contained in a liquid sequestering element.

Abstract: An allergy testing tray assembly has an outer tray and an inner tray fitted in the outer tray. Each one piece tray is molded to have three longitudinal areas separated by two rows of spaced posts. A plurality of allergy testing needles are removably held between the adjacent posts. These syringes each have needle protective housing and a sheath that covers the needle prior to use color coded to reflect the gauge of the needle of the syringe. The plunger end of each of the syringes is capped so that each syringe is isolated from the environment. The trays are sealed by a cover sheet that may also have markings in the same color as the color of the housing and the sheath, so that a clinician can readily tell the gauge of the needle of the syringes stored in the trays, without having to remove the cover sheet.

Abstract: A rigid crush resistant plastic tube having quickly removable end caps. A hypodermic needle contained in a sterile needle wrapper is placed inside the crush resistant tube so that a portion of the wrapper is folded over the outside distal end of the tube. The end cap is then secured over the folded wrapper portion on the distal end of the tube in a friction fit arrangement to secure the needle wrapper between the cap and tube. In this arrangement, when the end cap is removed, it pulls the needle wrapper out of the protective plastic tube to allow for rapid access and deployment. In use, the plastic tubes are secured with elastic bands inside a carrying case, such as a first aid backpack. As the soft cases are often subject to substantial exterior impacts, the tubing significantly reduces the risk of needle breakage.

Abstract: A bone cement injecting tool is configured to be capable of inhibiting or preventing the occurrence of air bubbles in the liquid as a pressure transmitting medium. The bone cement injecting tool is composed of a first cylinder possessing a bore, a second cylinder possessing a bore, a first gasket slidably sealing the bore of the first cylinder, a second gasket slidably sealing the bore of the second cylinder, a tube communicating the first cylinder and the second cylinder, and liquid (e.g., water) filling the space I the tube and the first and second cylinders between the two gaskets. A piston is positioned in the first cylinder, and a pressure-retaining member applies pressure to the forward end of the piston so the piston moves the first gasket toward the forward end, thereby delivering the water to the second cylinder through the tube. During storage, the pressure-retaining member pushes the piston toward the fore-end, and this pushing force produces the pressure of the water.

Abstract: A package is described having two blanks of a sheet material joined along edges to form one or more enclosed compartments to retain a urinary catheter. The joined edges provide at least one peeling zone permitting separation of two foil walls. A gripping means is provided to allow a firm grip relative to the peeling zone.

Abstract: A syringe has a barrel to receive a cartridge. The barrel has a front end portion to which a needle is connected for engagement with the cartridge. At its rear end, the barrel has a plunger mechanism. A sleeve is slidably mounted on the barrel and can be pushed forwards to sheath the needle. The needle is mounted on the barrel via a push-fit mounting device. The needle can be removed for disposal in a container by inserting the syringe into a tube on top of the container so that the protective needle sleeve is pushed back and the needle and mounting device pass through a collar of gripping fingers at an inner end of the tube. The fingers catch behind the mounting device so that this is pulled off to drop into the container with the needle when the syringe is withdrawn from the tube.