Abstract: The injection device comprises a medicine container, means for injecting medicine from the medicine container to a patient through a needle, a skin contact surface crossable by the needle and having protrusions which are pressed around the injection site when the injection device is applied on the patient's skin for the injection, the protrusions being arranged so as to reduce the pain caused by the penetration of the needle, and a sensor for detecting contact of the patient's skin with the skin contact surface, wherein a predetermined force of application of the injection device on the patient's skin is required for the sensor to detect the patient's skin.

Abstract: In some embodiments, without limitation, the invention comprises a catheter having an elongated housing with a channel disposed therein. A laser delivery member is movable and at least partially disposed within the channel. A ramp is disposed within the housing at an angle to its central axis and proximate to its distal end. The ramp is adapted to move the distal end of the laser delivery member outwardly from the central axis of the housing. A guidewire biases the distal end of the laser delivery member generally inwardly toward the central axis of the housing. In some embodiments, without limitation, the offset of the central axis of the tip of the laser delivery member from the central axis of the housing is determined by adjusting the extent to which the laser delivery member travels on the ramp, and disposition of the laser delivery member on the guidewire maintains the offset tip substantially parallel to the central axis of the housing.

Abstract: A reader system for reading information on at least one identification tag associated with a syringe connected to a fluid injector has a detector and a background screen spaced apart from the detector such that at least one of the at least one identification tags is positioned in an optical path between the detector and the background screen when the syringe is connected to the fluid injector. The reader system further has an illumination system configured for illuminating at least a portion of the background screen. The detector is configured for detecting and decoding the at least one identification tag.

Abstract: Apparatuses, systems, and methods are provided for securing an intra-osseous device within a safety device to prevent stick injuries and to guide the removal of the intra-osseous device from the bone of a patient. A body of the safety device has a cavity that receives the intra-osseous device, and the cavity guides the removal of the intra-osseous device along a straight line to prevent injury during removal. The intra-osseous device is drawn past a lock feature that secures the intra-osseous device within the body such that a needle of the intra-osseous device is contained within a cavity of the body and cannot injure the patient, staff members, etc.

Abstract: Devices and methods for preventing reperfusion injuries when an occlusion balloon is deflated. A catheter having an infusion lumen exiting the catheter distal of a stent balloon and/or occlusion balloon allows a therapeutic agent to be introduced to a target location to establish desired temperatures and pressures prior to deflation of the balloon such that negative effects of reperfusion are minimized.

Abstract: A catheter assembly may include a catheter, catheter adapter, needle, needle guard, and housing. The housing may be coupled to the needle guard and disposed within a lumen of the catheter adapter. The needle guard may include first and second resilient arms, which may include first and second curved portions, respectively. When the needle is in a ready position, the first and second curved portions may be urged by a shaft of the needle into retaining contact with an inner wall of the catheter adapter. When the needle is in the retracted position, the shaft may no longer bias the first and second resilient arms outwardly such that the retaining contact between the first and second curved portions and the catheter adapter is released, and the housing and the needle guard enclose a distal tip of the needle.

Abstract: A sealed fluid transfer device comprised of tubing, a proximal fitting, and a distal needle assembly is provided. The needle assembly includes a needle hub secured to a needle cannula. A cantilevered actuator arm extends outwardly from the needle hub having an actuator button at its free end. The needle assembly is disposed in a barrel and can move from a distal position, where the needle is exposed, to a proximal position, where the needle is shielded. The barrel includes a septum which seals the barrel. A spring is disposed in the barrel for propelling the needle assembly to the proximal position. The barrel includes an aperture that receives the actuator button for locking the spring in a compressed condition. Depression of the actuator button enables the spring to propel the needle assembly into its proximal position. A safety mechanism prevents inadvertent depression of the actuator button.

Abstract: Methods of selecting or designing an implant to be used in a patient are provided. A CT scan of a patient's mouth is performed. A 3D CAD model of the patient's mouth is created utilizing data generated by the CT scan. Properties of the patient's mouth are determined based upon CT scan data and assigned to the 3D CAD model. A desired location for an implant is selected. A FEA simulation is performed on the 3D CAD model to choose an implant or to design an implant that optimizes a selected variable.

Abstract: A system for injecting includes a syringe body defining a proximal opening and a distal needle interface. The system also includes a plunger member defining a plunger interior and configured to be manually manipulated to insert a stopper member relative to the syringe body. The plunger member includes a needle retention feature disposed in the plunger interior, an energy-storage member disposed in the plunger interior, and an energy-storage member latching member disposed in the plunger interior. The system further includes a needle hub assembly coupled to the distal needle interface of the syringe body. The needle assembly includes a needle having a needle proximal end feature, a hub, and a needle latching member configured to couple the needle to the hub. The needle is retractable into plunger interior upon manipulation of the plunger member to actuate the energy-storage member latching member.

Abstract: Needle assemblies are generally discussed herein with particular discussions extended to needle assemblies having a tip protector with a plurality of wall surfaces for preventing contact with the needle tip from a side. Aspects of the tip protectors discussed herein include a first protector body having an arm for blocking a needle tip surrounded by a second protector body having a plurality of wall surfaces.

Abstract: An auto-injector having a body (1) receiving a reservoir (S) and including a piston (P); a piston rod (5) movable between a primed position and an injection position in which the piston rod (5) has moved the piston (P) to inject fluid into an injection site; and a visual, audible, and/or tactile indicator device for indicating that the autoinjector may be removed from the injection site. The autoinjector includes a retarding system to delay actuating the indicator device relative to the end of injection and that includes a dashpot (16), a shear member (19) and a fluid. The dashpot or the shear member is rotatably mounted in the body and the other is stationary in rotation, the turning of one relative to the other being braked by shearing the fluid contained in the dashpot. The dashpot and shear member include projections that impede the flow of the fluid.

Abstract: Medical device assemblies capable of aspirating liquid into a syringe barrel or other medical devices while evacuating any air from the syringe are described. An exemplary medical device includes a syringe barrel, plunger rod and stopper assembly having an air permeable and liquid impermeable porous portion and structure for forming a vacuum within either the stopper or the plunger rod. Described is a medical device including a syringe barrel, plunger rod and stopper assembly having an air permeable and liquid impermeable porous portion and structure for forming a vacuum within chamber between the stopper and plunger rod wherein the plunger rod includes a sealing edge and is moveable relative to the stopper. Exemplary medical devices may include a vent for allowing air that permeates through the porous portion to escape to atmosphere. Methods for aspirating a syringe barrel with a liquid are also provided.

Abstract: A needle tip storage and removal device comprises a storage compartment having a splined socket which engages complementary splines on a needle tip collar, the storage compartment being sealed by a peelable foil. Alongside the storage compartment is a removal compartment having a drive socket of similar configuration. The device assists safe removal and disposal of a used needle prior to fitting a new needle.

Abstract: An injection device includes a housing; a receptacle for injection fluid; a dosing piston to press out the injection fluid; a feed part connected to the dosing piston via a first threaded connection; a slide having a thread of a second threaded connection; and, a setting part having a thread of a third threaded connection and configured to set an amount of injection fluid to be dispensed. The setting part moves in the distal direction by virtue of the third threaded connection when the amount of injection fluid to be dispensed is being set. The setting part can move in the proximal direction when the injection fluid is pressed out. A latching unit defines a latching position of the setting part and acts between the setting part and housing. Each latching position has an unequivocal rotational position of the setting part in relation to the housing assigned thereto.

Abstract: The present invention relates to a medicament delivery device comprising a housing, a compartment inside said housing for positioning a medicament container, an injection needle arranged to said housing, being connectable to said medicament container for delivering a dose of medicament, a manually operated activation mechanism for activating said device, an actuation mechanism operably connected to said activation mechanism and arranged to, upon activation of said activation mechanism, extend said injection needle from a first position inside said housing to a second position wherein a penetration of a patient is performed, a plunger rod arranged in said housing capable of acting on said medicament container for delivering a dose of medicament through said injection needle, a driver capable of acting on said plunger rod for delivering a dose of medicament.

Abstract: An apparatus for use with a syringe for providing a safety syringe, the apparatus including a sheath (100; 300; 500) deployable for at least partially covering a needle (126) of the syringe; and a sheath actuator (102; 302; 502) for deploying the sheath by interaction with a sheath deployment mechanism (104; 304; 504); the sheath being configured to be stationary in relation to the needle until a syringe plunger (116; 316; 516) reaches a sheath release point on its inward stroke, and the sheath actuator being configured for deployment of the sheath on movement of the sheath actuator relative to the syringe plunger after the sheath release point.

Abstract: An automatic medication injection device including a driver (95), a retractor (190, 230) and a blocking member (180). Upon device triggering the driver is shifted proximally to move a device syringe, expel medication from the syringe0, and then to disengage itself from the syringe plunger. The driver and the blocking member have a complementary camming configuration by which the blocking member, during the driver shifting, is automatically rotated from a first rotational orientation to a second rotational orientation. The blocking member blocks retraction of the retractor when disposed in the first rotational orientation, and permits retraction of the retractor when disposed in the second rotational orientation, which retractor retraction withdraws the device syringe from an injecting position to a retracted position.

Abstract: The invention provides a safe auto-needle device for injection, comprising: a main housing and a syringe-support receiving a disposable prefilled syringe terminating in a needle covered by a needle sheath (NS). The speed of depressing of the syringe plunger is manually controllable by a user. In a first embodiment, a locking mechanism is present, for preventing premature advancement of the needle. A second embodiment comprises an interlock, for preventing depressing of a plunger, prior to advancement of the syringe-support to a needle penetration location. Additional components include a drive mechanism; and a needle shield moveable between: a needle covered position; a partially exposed position, to a fully extended needle safe position. The invention also discloses a needle sheath (NS) remover.

Abstract: An auto-retractable syringe having a barrel and a plunger wherein engagement of said plunger with an otherwise immobilised needle hub allows a biasing member to push the needle hub into a cavity in the plunger.

Abstract: In one aspect, a safety pen needle assembly includes a hub having an open proximal end, a needle fixed to said hub, said needle having a distal end for insertion into a patient, and a proximal end extending into said open proximal end of said hub, a shield having a distal opening and an internal thread that is engaged to said hub so as to be manually movable relative to said hub to selectively expose said distal end of said needle via proximal movement of said shield and cover said distal end of said needle via distal movement of said shield, said shield having an open distal end, and a cap that seals the distal opening of the shield.

Abstract: The invention pertains to a kit for assembling a disposable applicator for inserting an implant, in particular a rod-like implant containing an active substance, under the skin of a human or animal, the kit comprising a first component, in turn comprising a main housing part providing a handle for grasping and maneuvering the applicator, a cannula, and a cannula holder mounted in the main housing part, the main housing part having an opening which allows introduction of an implant into the proximal end of the cannula or the cannula holder, and, a second component for closing said opening, in turn comprising a second housing part and a rod attached to or forming an integral whole with the second housing part and mountable inside the cannula or the cannula holder.

Abstract: A passive safety needle device is disclosed having a housing, a needle hub, a needle cannula, a retractable sheath, a spring to bias the retractable sheath in a distal direction to cover the distal end of the needle cannula, a radial protrusion to cause the spring to move from the proximal spring position to the distal spring position, and a catch to secure the distal end of the spring to the distal end of the housing. The spring may bias the retractable sheath in a distal direction to cover the distal end of the needle cannula. The radial protrusion causes the spring to move from a proximal spring position to the distal spring position towards the catch located at the distal end of the housing.

Abstract: A needle assembly, comprising hub, a needle fixedly connected to said hub, an outer cover for removably receiving said hub and said needle, said outer cover covering a first end of said needle and an inner shield adapted to be connected to said hub for covering a second end of said hub.

Abstract: A telescoping syringe suitable for use with medications and other materials is presented. The telescoping syringe includes a valve, a plunger, and a barrel. The valve further includes a barrier, an outlet(s) through the barrier, and an annular extension extending from the barrier. The plunger further includes an inlet(s) and a first side wall with a proximal wall. The barrel includes a second side wall with a distal wall at one end and an open end at another end. The plunger is extendable from and retractable into the barrel at the open end via slidable engagement between first and second walls. The valve directly contacts one end of the first wall so that an annular flange slidingly engages an annular groove. The valve and the barrel slidingly contact the plunger so as to open and to close the inlet(s) and/or the outlet(s).

Abstract: A safety needle device is disclosed having a hub, needle cannula, housing, tether, retractable sleeve, locking member and spring element. The tether is movably disposed in the housing, the tether having a slot with an enlarged first guide path and a narrowed second guide path extending distally from the enlarged first guide path. The retractable sleeve is configured to move from an initial position to partially expose a distal tip of the needle cannula, a retracted position to fully exposes the needle cannula, and an extended position to fully cover the distal tip of the needle cannula. The proximal movement of one or more protrusions on the retractable sleeve, rotates the tether to move the at least one or more protrusions from the enlarged first guide path of the tether to the narrowed second guide path of the tether, this rotation activating the device.

Abstract: A syringe packaging system that includes a tube and a cap for enclosing a pre-filled syringe is disclosed. The tube includes a tube cut flange and the cap includes a cut skirt. With a syringe barrel contained within the tube, a syringe barrel cut flange is aligned with the tube cut flange. With the pre-filled syringe enclosed within the tube and the cap, the cut skirt of the cap surrounds the syringe barrel cut flange. In one embodiment, a film is securable to a portion of the tube and a portion of the cap to connect the tube and the cap with the pre-filled syringe enclosed within the cap and the tube.

Abstract: An apparatus for depositing an extrudable substance comprises a bracket and a sleeve, comprising an inner tubular sleeve wall and an outer tubular sleeve wall. The sleeve is coupled to the bracket and is rotatable relative to the bracket. The apparatus also comprises a cartridge, comprising an inner tubular cartridge wall and an outer tubular cartridge wall. The cartridge is configured to be positioned between the inner tubular sleeve wall and the outer tubular sleeve wall. The apparatus also comprises a valve, configured to be communicatively coupled with the cartridge, a nozzle, configured to be communicatively coupled with the valve, a linear actuator to control flow of the extrudable substance from the valve to the nozzle, an annular plunger, positioned between the inner tubular cartridge wall and the outer tubular cartridge wall, and a push-lock pressure cap, configured to be hermetically coupled with the cartridge.

Abstract: A syringe assembly may include a plunger having a stopper. A barrel may be configured to receive the plunger at an open first end. A tip cap may be removably attached to the second end and may form a chamber within the barrel between the plunger and tip cap. The chamber may be configured to contain a sterilization sensitive material. The barrel may be formed of a plastic material having a high barrier property configured to create a barrier between the sterilization sensitive material and gases produced for sterilization purposes such that the sterilization sensitive material remains unchanged during a sterilization procedure.

Abstract: An autoinjector having a body (1) receiving a reservoir (S) containing fluid and a piston (P); a piston rod (5) movable by an injection spring (8) between a primed position and an injection position; and a visual, audible, and/or tactile indicator for indicating the autoinjector may be removed from the injection site. The autoinjector including a retarding system for delaying actuation of the indicator relative to the end of injection, and including a dashpot (16) containing a fluid, a piston (19) in the dashpot, the dashpot or the piston movable in the body during actuation of the retarding system with the other stationary relative to the body, resulting in the fluid moving out from the dashpot through a flow passage (161; 195) to brake movement.

Abstract: Apparatus and methods for introducing a solid or semi-solid intraocular drug-containing implant into the anterior chamber of an eye are described. The drug-containing implant can be a rod-shaped biodegradable implant that may provide for the extended release of the drug and may be effective for treating a medical condition of the eye. The apparatus is ergonomically designed in the shape or style of a pen with tactile surfaces for easy gripping, a needle-rotation knob to permit orientation of the needle bevel in relation to the eye, and a spring-actuated mechanism for consistent deployment of the implant.

Abstract: An apparatus for depositing an extrudable substance comprises a bracket and a sleeve, comprising an inner tubular sleeve wall and an outer tubular sleeve wall. The sleeve is coupled to the bracket and is rotatable relative to the bracket. The apparatus also comprises a cartridge, comprising an inner tubular cartridge wall and an outer tubular cartridge wall, wherein the cartridge is configured to be positioned between the inner tubular sleeve wall and the outer tubular sleeve wall. The apparatus additionally comprises a valve, configured to be communicatively coupled with the cartridge, a nozzle, configured to be communicatively coupled with the valve, a linear actuator to control flow of the extrudable substance from the valve to the nozzle, an annular plunger, positioned between the inner tubular cartridge wall and the outer tubular cartridge wall, and a twist-lock pressure cap, configured to be hermetically coupled with the cartridge.

Abstract: A needle assembly for sampling fluid from a patient including a needle guard, an insertion needle, and a needle housing. The distal end of the needle guard includes a nose portion and a flexible nose extension defining a fluid collection reservoir. The proximal end of the needle guard includes a push feature. The insertion needle has a sharpened distal tip, a proximal needle end and a shaft defining a lumen extending therebetween. The needle housing is operably coupled to the proximal needle end and is slideably coupled to the needle guard. The needle housing includes a flash chamber including a wall defining a cavity. The cavity is in fluid communication with the lumen of the insertion needle and is sealed at one end by a gas permeable flash plug. The push feature selectively engages the flash plug to divert captured bodily fluids to the fluid collection reservoir for sampling.

Abstract: The safety syringe assembly is for inserting a needle into a patient and comprises a needle hub assembly and a safety cover. The needle hub assembly includes a needle, needle hub, and hub flex unit. The needle is mounted on the front side of the needle hub while the rear side is for receiving a syringe. The safety cover houses the needle hub assembly in a first position during shipping, a second position during insertion of the needle into the patient, and in a third position after the needle has been inserted into the patient while awaiting disposal. A portion of the safety cover includes magnification enabling a user to view a dosage calibration scale, needle bevel and air bubbles. The hub flex unit assumes a first enlarged position during shipping, is compressed during insertion into the patient, and slides into a third position after usage while awaiting disposal.

Abstract: A pneumatically activated retractable-needle syringe comprising a syringe barrel, a plunger, a needle, a needle hub, a locking tip, a propellant gas release cell and a rupture mechanism is provided. The plunger has a retraction lumen defined therein for receiving the needle when the retractable-needle syringe is actuated.

Abstract: The disclosure relates to a needle assembly adapted to couple with a medicament delivery device including a needle having a proximal tip and a distal tip, a needle hub coupled to the needle, a body adapted to engage the needle hub, a removable needle cap adapted to cover the distal tip, and a removable sealing element. The sealing element is adapted to seal an open proximal end of a compartment of the body, including the proximal tip, in such a manner that the proximal tip is housed in a sealed environment before use of the needle. The disclosure further relates to a medicament delivery device including such a needle assembly.

Abstract: A retractable needle catheter insertion device is provided with a cannula and a needle positioned within the cannula to assist with insertion of the cannula. After insertion of the cannula into a patient, the needle can retract into a protective sleeve that contains the needle in order to reduce the chance that a medical practitioner will be inadvertently stuck by a used needle. The needle is carried by a needle support that is slidably disposed within the sleeve. A spring biases the needle support and needle toward a retracted position, and the device also includes an activation hub that works in conjunction with the needle support to control retraction of the needle. The retraction may be activated manually by the medical practitioner or may be activated automatically. A modular system and method of manufacturing is also provided in which catheters having either manually or automatic retraction can be manufactured using common parts.

Abstract: A fluid injecting system (100) comprising an injector (A) having an injector body (10), a plunger shaft (30), a plunger assembly (20) having an inner plunger barrel (21) slidable within an outer plunger barrel (22), a fluid-cartridge (B) having a fluid (53) and a hypodermic needle (72) for injecting the fluid (53) at an injectable site. The fluid-cartridge (B) is configured to releasably engage with the injector (A). A vacuum (V) is created between the outer plunger barrel (22) and the inner plunger barrel (21) upon formation of a united plunger barrel (40). Also, forward movement of the united plunger barrel (40) transfers the fluid (53) from the fluid-cartridge (B) into the injectable site. The hypodermic needle (72) retracts within empty fluid-cartridge (B) due to release of the vacuum (V) and the injector (A) is disengaged from the fluid-cartridge (B) for reuse. Further, a fluid injecting method (300) is provided.

Abstract: A catheter assembly comprises a catheter (18), a needle (12) having a sharp distal tip disposed within the catheter (18), a catheter hub (14) connected to the catheter (18) having the needle (12) passing therethrough, the catheter hub (14) including a valve (38) that selectively permits or blocks a flow of fluid through the catheter (18), a valve actuator (54) that moves between a first position and a second position, and a return member (56) that returns the valve actuator (54) from the second position to the first position, and a needle protection member (176) that encloses the sharp distal tip of the needle (12).

Abstract: A novel single use auto-injector for delivering a fixed amount of medicament is described. The auto-injector may include a sealed housing rotatably held in a cover. Once the auto-injector is positioned at the injection location, the user can transition the housing from a locked to an armed position. The user can then compress the sealed housing into the cover, triggering activation mechanisms that initiate the injection. A first activation mechanism engages an interlock to prevent reuse of the auto-injector. A second activation mechanism straightens and extends a curved needle to a set the exposed needle length. A third activation mechanism pierces a sealed reservoir allowing the medicament to be forced through the injection needle. Following the injection, the auto-injector expands and interlocks, retracting the needle into the auto-injector and preventing reuse.

Abstract: An auto injector having sequential control of needle insertion and dose injection is disclosed. A syringe with a needle is movably positioned in a housing between a first position in which the needle is accommodated inside the housing and a second position in which the needle protrudes outside the housing. A plunger rod tube has at least one locking member configured to normally lock a plunger rod to the plunger rod tube. A syringe driver applies a force to the syringe to move the syringe together with plunger rod tube, plunger rod and plunger rod driver from the first position to the second position. In the second position, the locking member is unlocked and releases the plunger rod to thereby activate the plunger rod driver to advance the plunger rod in the syringe for delivering of at least one dose of medicament.

Abstract: A modular retractable needle assembly having a unitary propellant release structure is provided. The modular retractable needle assembly can be coupled to a suitable syringe. A modular filler needle can be provided that is engageable to the syringe. Kits comprising the modular retractable needle assembly, one or more syringes, and a modular filler needle are provided.

Abstract: A plunger locking assembly is provided for a syringe which has a barrel and a plunger. The barrel has a closed end with a cannula connector, an open end bounded by a peripheral lip and a barrel longitudinal axis extending between the closed end and the open end. The plunger has a plunger inner end, a plunger outer end and a plunger longitudinal axis extending between the plunger inner end and the plunger outer end. The plunger is slidably displacable within the barrel to different longitudinal lock positions and the barrel and plunger longitudinal axes are coextensive with one another. The plunger locking assembly includes a main body and a plunger locking mechanism. The main body has an inner end, an outer end and a main body longitudinal axis and is adapted to engage the plunger. The plunger locking mechanism is positioned on the main body and is adapted to lock the plunger at a fixed longitudinal lock position within the barrel to prevent further slidable displacement of the plunger into the barrel.

Abstract: A syringe holder includes: a barrel body that holds a syringe; a holder opening; deformation promoting portions; and radial movement-restricting portions. The radial movement-restricting portions are provided close to the deformation promoting portions. Being brought into contact with first portions, the radial movement-restricting portions restrict the syringe from moving in a radial direction with respect to the barrel body.

Abstract: A percutaneous access device for use in minimally invasive surgery includes an elongated body having a proximal portion and an opposing distal portion. The proximal portion has a proximal bore extending therethrough and the distal portion has a distal bore extending therethrough. The distal portion of the body is hingedly connected to the proximal portion in a first percutaneous access position and a second anchoring position. In the first percutaneous access position the distal and proximal bores are linearly aligned when a surgical instrument is inserted into both the proximal and distal bores. In the second anchoring position the distal bore is angularly displaced from the proximal bore when the surgical instrument is removed from the distal bore.

Abstract: Disclosed is a method for assembling a safety device and mounting the safety device on a syringe member before the syringe member is filled, said method comprising the steps of: providing a sleeve, a spring element and a mounting element; introducing the spring element into the sleeve along a mounting direction; introducing the mounting element into the sleeve along the mounting direction; obtaining the safety device; before the syringe body is filled, mounting the safety device on the syringe body by connecting the mounting element to the syringe body.

Abstract: An enteral dosing control coupling comprising a cylindrical collar defining a hollow internal chamber and a lumen extension tip projecting axially into the internal chamber, the lumen extension tip defining an internal lumen extending therethrough. In example forms, the lumen extension tip is integrally formed with the cylindrical collar. In other example forms, the lumen extension tip is a separate piece and is removably engageable within the cylindrical collar. In some example forms, the present invention relates to syringes, connectors, couplings, etc. having ISO 80369-3 formatted couplings. In other example forms, the present invention relates to connectors, couplings, etc. for adapting coupling formats other than the ISO 80369-3 coupling format to the ISO 80369-3 coupling format.

Abstract: A single-use needle cover configured to obscure, protect, or hide at least a portion of a needle from view before, during, and/or after an injection and/or aspiration procedure is disclosed. In some embodiments, the cover includes a housing at least partially containing the needle and configured to couple to a syringe, wherein the housing includes an axis and a guide member. In some embodiments, a sleeve has a plurality of tracks configured to slidingly receive the guide member, wherein the sleeve is configured to retract, extend, and rotate with respect to the housing. In some embodiments, after the sleeve has been retracted and extended one time, a first locking member inhibits further retraction of the sleeve and a second locking member inhibits rotation of the sleeve.

Abstract: Catheter assemblies are generally discussed herein with particular discussions extended to catheter assemblies having a tip protector, a valve, a valve opener, and optionally a needle wiper. The valve opener is disposed inside a catheter hub and is configured to be pushed by an IV set luer connector to open a valve following successful catheterization to pass fluids or other solutions through the catheter. A tip protector is incorporated to block the needle tip and prevent the same from accidental needle stick. A wiper is optionally included to wipe blood deposits from the needle when the same is retracted from the catheter.

Abstract: An automatic retractable syringe comprised of a syringe inside a compressed spring loaded locking safety sheath that moves into a protective position over the needle of the syringe that is triggered by the depression of the plunger, causing the positional locking mechanism to displace from its initial position and activate a compressed spring that expands, moving the locking safety sheath into its protective position and locks the sheath, preventing further movement of the locking safety sheath. An optional fusing system acts to permanently fix the locking mechanism in place to further secure the locking safety sheath in the protective position.

Abstract: The invention relates to a safety device for a syringe for avoiding stab wounds, said syringe having a syringe body and a piercing means arranged on the distal end of the syringe body. The safety device comprises a sleeve element that extends along an axial direction (X) and encloses at least partly the piercing means and the syringe body, and a collar element that can be arranged on a distal end region of the syringe body and locks the safety device in the axial direction (X), said collar element having at least one guide projection which engages at least one guide track of the sleeve element. The safety device is further characterized by having a cap element that can be arranged at least in sections on top of the sleeve element and by means of which the sleeve element can be locked with respect to the movement of the syringe body relative to the sleeve element.