Abstract: An adapter mountable to a retractable syringe barrel comprises a body that includes a needle portion and a barrel-engaging portion and a needle aperture. The adapter facilitates mounting a needle assembly to the barrel. The needle assembly comprises a needle body and cannula and an immobile, compressible needle seal, wherein the needle body and the needle seal are releasably engaged. The needle seal is engageable with a needle portion of the adapter. The needle body comprises one or more fluid reclaim channels that facilitate efficient delivery of the fluid contents of the retractable syringe. The retractable syringe also comprises dual locking systems to impede or prevent re-use.

Abstract: A safety syringe with a plunger in which a needle is attached to a mobile component that is mechanically not linked to the plunger but is slidable within the barrel of the syringe and has a valve mechanism for opening a port connecting the interior volume between the mobile component and the plunger to the needle bore. The mobile component is first pushed by the plunger to the bottom of the barrel so that the needle extends normally, the mobile component is mechanically locked in place for use conventionally, and the needle bore is opened. After use, the needle bore may be closed, the lock released, and the mobile component and attached needle sucked back into the barrel by pulling the plunger out, retracting the used needle into the barrel. There may be a plunger lock. There may be an upper barrel locking position for the mobile component.

Abstract: A device for delivering a medicament intradermally includes a cartridge (112) having a first end (110) and a second end (114) and defining a volume (111) therebetween. The volume (111) is adapted to contain the medicament. A driving member (121) has a first end (126) and a second end (128). The first end (126) of the driving member (121) is disposed in the cartridge (112) and the second end (128) of the driving member (121) is disposed outside the cartridge (112). A stopper (115) is slidably disposed in the cartridge volume (111). The driving member (121) is releasably disposed in the stopper (115) such that when the driving member (121) is retracted from the cartridge (112) the stopper (115) is disengaged from the driving member (121) and remains in the cartridge volume (111).

Abstract: The invention relates to a needle tip guard for a safety IV catheter assembly comprising a catheter tube having a distal end and a proximal end; a catheter hub having a distal end and a proximal end, wherein the distal end is joined to the said catheter tube and the proximal end defines a chamber; a needle extending through the catheter hub and the catheter tube having opposite proximal and distal ends defining an axial direction A, wherein the proximal end is joined to the needle hub and the distal end forms a sharp tip and a change in profile is provided between the proximal and distal ends of the needle; and a tip protector assembly movably arranged in between the catheter hub and needle hub on the needle such that the tip protector assembly is retained partially and/or completely in the chamber of the catheter hub and wherein the tip protector assembly is configured to entrap the needle tip upon withdrawal of the needle from the catheter hub.

Abstract: An insertion device, generally used with an infusion set, including a needle being adapted for puncturing at one end and including at the opposite end a hub. The hub includes a handle part and a guard part that are capable of securing the needle through the use of locks. Locking structures are used to secure the insertion device in a position where the needle is covered in a locked position, avoiding unintended contact with the needle.

Abstract: Device (1a, 1b, 1c, 1d; 40) for extracting, storing and/or processing blood or other substances of human or animal origin, and for applying blood compounds or other biological compounds, which comprises a body (2; 41) inside which a piston (3; 42) is capable of moving longitudinally and is separable at least in part, where the body (2; 41) is provided with an internal space (9; 51) that may be connected to the outside by means of a conduit (6; 50) at a first end (4; 48) of the body (2; 41), where the body (2; 41) and the piston (3; 43) may be blocked longitudinally in at least one position to allow the creation of different degrees of vacuum. The device has multiple uses and is extremely versatile.

Abstract: A retractable syringe is proposed having a cutting head mounted on a plunger of the syringe. When the plunger is advanced to expel fluid from the syringe, the cutting crown cuts a retention mechanism which holds a needle unit of the syringe, allowing a drive mechanism to drive the needle unit into the syringe. The cutting crown is shaped to reduce the force which has to be applied to cut the retention mechanism. Furthermore, a disposable needle assembly for attachment to a syringe unit is proposed. The disposable needle assembly has a needle and connector element for connecting the needle to the syringe unit. The connector element encircles the needle and has a thread on its outer surface for mating with the syringe unit.

Abstract: A lancing device for collecting body fluid samples with a body at the end of which an endcap is arranged. The endcap has a positioning surface with an outlet opening. The device further comprises a socket to receive at least one lancet, which is interchangeably clamped in the body, a clamping device, and a release mechanism, with which the lancet is clamped inside the body. The lancing procedure is initiated with the tip of the lancet emerging through the outlet opening. An ejection device is used to eject a used lancet. The endcap is functionally coupled with the ejection device in such a way that, when the ejection device is actuated, the endcap is held pivotably on the body so that it can swing out of the path of the lancet.

Abstract: A syringe including a barrel and a plunger slidably disposed within the barrel is disclosed. A distal end of the barrel defines a roof, and an elongate tip, in fluid communication with the barrel, extends from the roof. A protrusion forming a ridge may be disposed on one of the roof of the barrel and the plunger head. When the plunger head contacts the roof, the protrusion forms a channel between the plunger head and the roof. The channel isolates fluid within the channel from the elongate tip, which in turn reduces the spray of fluid through the distal end of the syringe. In another embodiment to reduce the spray of fluid through the distal end of the syringe, an impulse reduction system may be used to reduce or prevent the proximal portion from applying a distally directed impulse to the distal portion after the breakable connection is broken.

Abstract: An IV catheter introducer assembly including a catheter hub defining a chamber; a tubular member extending distally from the catheter hub having a length and defining a lumen, the lumen being in fluid communication with the chamber and configured to removably receive an introducer needle. The device also including a retention member disposed within the chamber having a body having a central lumen having a longitudinal length extending along a lengthwise direction to the length of the tubular member and sized to seal against an introducer needle. The retention member including a venting channel having at least a portion formed as a conic helix traversing a surface of the retention member along a radial path to the lengthwise direction.

Abstract: An injector folding and injecting a flexible intraocular lens into the eye of a patient is described. The injector is configured to be loaded with the intraocular lens, and optionally, an aqueous solution, before the injector and lens are sterilized. The injector includes a lens compartment that is configured to prevent leakage of the aqueous fluid from the lens compartment caused by autoclaving/sterilization.

Abstract: A replaceable needle assembly is provided for a retractable, prefilled syringe comprising a barrel having a mounting member and a plunger, whereby the retractable needle can be replaced by a user without affecting the retraction mechanism. The replaceable needle assembly comprises a needle fitted to a retractable needle mount and a needle retainer. The needle mount is removably, screw-threadedly mountable to the mounting member of the barrel. The needle retainer comprises a plurality of fingers that releasably engage the retractable needle to thereby prevent inadvertent retraction of the retractable needle before engagement by the plunger. The plunger comprises a plunger seal comprising an outer member and an inner member that engages the needle for spring-driven retraction. At the end of retraction, a lock is formed between the plunger and barrel to prevent re-use of the syringe.

Abstract: The invention relates to a needle guard for use in a medical device, in particular for use in a catheter device, including a base portion having a needle passage extending in an axial direction from a proximal side of said base portion through said base portion to a distal side of said base portion wherein a needle shaft having a principle outer profile can be movably arranged in said needle passage; first and second arms extending substantially in said axial direction from said distal side of said base portion, wherein said first arm has a distal region and a proximal region; and a distal wall transversely arranged at said distal region of said first arm. The invention further relates to a catheter apparatus including such a needle guard and a needle.

Abstract: The present invention concerns a medical pump comprising: a. A hard housing comprising a top (24) and bottom (1) hard shells, within which a rigid wall (3) and a movable membrane (2) create three distinct chambers; wherein i. said movable membrane tightly separates said second (29) and third (22) chambers ii. said first and third chambers have a watertight interface iii. said second chamber (29) is designed to contain a fluid iv. said first chamber (23) comprises a first venting mean (20) which is arranged to provide a fluidic communication between said first chamber (23) and the external environment; v. said third chamber (22) comprises a second venting mean which is arranged to provide a fluidic communication between said third chamber (22) and the external environment b. A pumping element (4) located in the first chamber (23) c. A least one pressure sensor which measure the pressure gradient between the first chamber (23) and the second chamber (29) d. A fluid pathway which permits: i.

Abstract: An injection needle assembly includes a needle tube having a needle tip to be stuck into a skin, a first member, a second member, an adjustment portion, and a pressing force restricting member. The first member holds the needle tube and the second member holds the first member movably toward the axial direction of the needle tube. A discharge portion of the syringe is fitted into this second member. The adjustment portion is provided at the periphery of the needle tube and includes a needle protrusion surface which abuts the skin in a case in which the needle tube is stuck to the living body. The pressing force restricting member is arranged between the first member and the second member, and restricts the pressing force added from the first member to the skin.

Abstract: A syringe for dispensing anesthetic from a cartridge having an interior wall defining a hollow interior sized and shaped for receiving a dose of anesthetic, and a piston. The syringe includes a tubular plunger slidably received in the hollow interior of the tubular cartridge. The plunger has a hollow interior extending between a distal end shaped for engaging the piston and an open proximal end. The syringe includes a plunger rod slidably received in the hollow interior of the tubular plunger. The rod has a sharp distal end adapted to penetrate the piston, a proximal end, and a length extending between the distal end and the proximal end sized so a delivery portion of the rod extends through the piston into the cartridge when the rod is driven through the piston. The delivery portion includes a recess for receiving a buffering agent to reduce acidity of the dose of anesthetic.

Abstract: One embodiment provides a method of using contextual lighting to assist a user of a medical fluid injection system. In this embodiment, the method includes providing a lighted display in proximity to a component of the injection system during setup of the medical fluid injection system. If the user has properly performed a setup function that is associated with the component of the injection system, the method further comprises providing a first visual indication on the lighted display. If the user has not properly performed the setup function that is associated with the component of the injection system, the method further comprises providing a second visual indication on the lighted display.

Abstract: A replaceable needle assembly is provided for a retractable syringe comprising a barrel and a plunger, whereby the retractable needle can be replaced by a user without affecting the retraction mechanism. A mounting member is removably mountable to the barrel by way of a screw-thread connection and a needle mount is removably coupled to the mounting member. A needle is mounted to the needle mount. The barrel comprises a needle mount retainer that comprises a plurality of fingers that engage the retractable needle mount to prevent inadvertent retraction. The plunger comprises a collapsible seal which maximizes the efficiency of fluid delivery prior to the plunger engaging the retractable needle mount for retraction. An initially compressed spring decompresses to drive retraction of the plunger and the engaged needle mount. A lock formed between the plunger and barrel prevents further use of the plunger after retraction.

Abstract: An auto-injector for administering a dose of a liquid medicament comprising an elongate housing arranged to contain a syringe with a hollow needle and a stopper for sealing the syringe and displacing the medicament, the housing having a distal end and a proximal end with an orifice intended to be applied against an injection site. The syringe is slidably arranged with respect to the housing. A spring capable of, upon activation: pushing the needle from a covered position inside the housing into an advanced position through the orifice and past the proximal end (P), operating the syringe to supply the dose of medicament (M), and retracing the syringe with the needle into the covered position. After delivering the medicament, an activator arranged to lock the spring in a pressurized state prior to manual operation and capable of, upon manual operation, releasing the spring for injection.

Abstract: According to the invention, a safety device for a pre-filled syringe comprises of a needle shield adapted to cover an injection needle of the pre-filled syringe before and after an injection, a support body with at least one pivoting arm adapted to engage a barrel collar of the pre-filled syringe and an outer body with a first inner sleeve comprising a bevelled section. The needle shield, the support body and the outer body are telescopically arranged. The needle shield, the support body and the outer body may telescope with respect to each other to cover and to expose the injection needle of the pre-filled syringe. The bevelled section is arranged to abut against the pivoting arm connected to the support body by a living hinge to deflect the pivoting arm radially inwards, so that the pivoting arm may engage the barrel collar after a dose of a medicament contained in the pre-filled syringe has been disposed beneath the skin of a patient receiving the injection.

Abstract: A needle assembly (2) for a drug delivery device (1) comprises a needle seal (3), a needle retainer (4) and a needle (5). The needle retainer (4) secures the needle (5) against displacement with respect to said needle retainer (4) when a dose of drug is being delivered. The needle seal (3) is configured to push onto the needle retainer (4) after delivering the dose of the drug, thereby unlocking the needle (5) from the needle retainer (4).

Abstract: A hemostasis mechanism includes a housing, and a pressure responsive seal positioned within the housing and having an outer seal surface exposed to a fluid pressure of a port formed in the housing. A pressurization device is in fluid communication with the port, and includes a detent having a release state, and an engaged state holding a plunger of the pressurization device at an advanced position to maintain an increased fluid pressure supplied to the pressure responsive seal to maintain sealing engagement about a transluminal device. Related methodology is also disclosed.

Abstract: A single-use auto-disable syringe device utilizes a locking element to prevent re-use of the syringe by locking the plunger rod with respect to the barrel upon completion of an injection stroke. The plunger rod includes a plurality of teeth comprising distally facing shoulders provided on a majority of the length of an elongate portion of the plunger rod.

Abstract: A pneumatic retractable syringe has a plunger having an interior retraction lumen. The plunger and syringe barrel have cooperating locking elements so that the plunger is locked after use within the syringe barrel. After injection of medicament is completed, the needle is retracted into the lumen by compressed gas that is released from a gas cell within the syringe when the gas cell is ruptured just before the plunger reaches the end of its downstream path of travel.

Abstract: Described are passively activated safety needle assemblies and methods for use. The assemblies comprise an elongate hollow outer shield, an elongate hub slidably engaged within the outer shield and biased to move proximally with respect to the outer shield. A locking ring in the hub has a ring element that cooperates with an activation element on the outer shield rotate the locking ring and disable the assembly.

Abstract: A jet injector that includes a prefilled syringe. The syringe includes a fluid chamber that contains a medicament. The syringe also has an injection-assisting needle, and a plunger is movable within the fluid chamber. A housing is configured for allowing insertion of the needle to a penetration depth. An energy source is configured for biasing the plunger to produce an injecting pressure in the medicament in the fluid chamber of between about 80 and 1000 p.s.i. to jet inject the medicament from the fluid chamber through the needle to an injection site.

Abstract: An instrument, article and method are provided for minimizing pain during administration by injection of a liquid, such as, an anesthetic. The instrument has a forward end. A rod or lightpipe mounted freely for vibration projects out of the forward end. The article, a single use tip, is composed of a tip sleeve removably mounted on the forward end of the instrument and a tip member removably mounted on the projecting rod or lightpipe to vibrate a preselected injection site on a human or animal. The tip sleeve and tip member are covered by an elastic overmold that enables the tip member to vibrate freely with respect to the tip sleeve and light from the lightpipe to illuminate the injection site. The overmold of the single use tip is torn during removal of the single use tip from the instrument.

Abstract: A syringe with a blocking structure, and the structure includes a one-way engagement unit having a propping portion, a flange extended outwardly from a rod and abutted with a cylindrical body, and a flexible bracket extended outwardly from the rod and isolated from the propping portion, and the flexible bracket has an external diameter greater than the propping portion. When the rod is moved forward with respect to the cylindrical body to pass through the flange, the flange abuts the flexible bracket to tilt backward. When the rod is moved backward with respect to the cylindrical body, the flange abuts the flexible bracket to tilt the flexible bracket forward, and the propping portion blocks the flexible bracket.

Abstract: An intravenous catheter insertion device and method of use are described. The insertion device coordinates movement of an access needle, a coaxial intravenous catheter and a flexible safety guidewire. A vein is punctured with the access needle, then an actuation member on the insertion device is used to advance the safety guidewire into the vein. The safety guidewire allows the access needle and the intravenous catheter to be safely advanced into the vein. Then, the actuation member is actuated to simultaneously withdraw the access needle and the safety guidewire, leaving only the intravenous catheter in the vein. The intravenous catheter is then disconnected from the insertion device and connected to a source of intravenous fluid, medication, etc.

Abstract: A needle retraction apparatus for a medical device such as a liquid infusion or collection device, the apparatus having a body, a needle retraction mechanism seated inside the body, a transverse slide member with an external needle retraction chamber, and a retraction actuator that is rotatable relative to the slide member, the retraction actuator being attachable to or made as part of the liquid infusion or collection device, whereby rotation of the device causes the slide member to move in a linear translational direction to reposition the retraction chamber in alignment with the needle retraction mechanism and allow retraction.

Abstract: An injection device comprising a medicament container, a needle attached to the container, and a mechanism for automatic penetration of the needle, injection of medicament and withdrawal of the needle. The device operates by initiating a penetration sequence, followed by an injection sequence and followed by a withdrawal sequence. A previous sequence can trigger a subsequent sequence. The device further comprises a dampening mechanism arranged and designed to dampen the movement of the injection mechanism during an injection sequence.

Abstract: An apparatus and method for in vivo fertilization through self-insemination includes sleeve fabricated of soft silicone elastomer having a tubular portion and a distal bulbous head. The sleeve may be secured concentrically about a syringe approximating the size, configuration, and feel of a human penis. The bulbous head includes lobes arrayed at equal angles about the head, adjacent lobes being separated by narrow channels extending longitudinally to provide a flow space for air and fluids. The distal stem of the syringe extends through the sleeve at the distal end thereof. Thus seminal fluid discharged from the syringe will be ejected out of the central opening in the head of the sleeve.

Abstract: A housing component of a drug delivery device to accommodate a drive mechanism, wherein the drive mechanism is operable to interact with a piston of a cartridge containing a medicinal product to be dispensed by the drug delivery device. The housing component comprises at least one radially inwardly extending flange portion to be operably engaged with a piston rod of the drive mechanism, wherein that the flange portion is at least partially structurally strengthened.

Abstract: A cutting element for a retracting needle syringe having a plunger with a cuttable distal end and a spring biased needle held by a cuttable support and a cutting element capable of cutting the cuttable distal end and the cuttable support includes a body portion having a proximal end, a distal end side wall therebetween and a passageway therethrough. The distal end of the body portion includes a cutting edge and a raised distally projecting tapered cutting tooth having distally converging edges. At least one tooth edge includes a sharp side wall for cutting the distal end of the plunger and the needle support.

Abstract: An I.V. flush syringe assembly includes a barrel having an inside surface defining a chamber for retaining fluid, an open proximal end and a distal end with a passageway therethrough in fluid communication with the chamber. An elongate plunger having a proximal end, a distal end and a flexible stopper is slidably positioned in fluid-tight engagement with the inside surface of the barrel for drawing fluid into and out of the chamber by movement of the stopper relative to the barrel. The barrel includes anti-reflux structure for holding said stopper in a partially deflected position after has been delivered from the chamber and the stopper is being force against the distal end of the chamber.

Abstract: The invention relates to devices used in the fields of drag delivery or sampling. More particularly, it relates to a disposable assembly which is fitted to an actuator device which causes the skin piercing element to enter the skin to deliver a drug (or other substance) or take a sample. Preferably the assembly is “made safe” after actuation, such that the disposable assembly can't be reused and more preferably still the skin piercing element is safely housed in the assembly such that it does not constitute a “sharps” risk.

Abstract: The present invention relates to a device for automatic injection of a product into an injection site, the device comprising: a container having a displaceable piston; a tubular housing having at least a flexible part which, in a rest state, defines a first opening; a piston rod; and, an intermediate part fixed to the piston rod which defines a diameter larger than the first opening. With sufficient distal displacement of the piston rod, the intermediate part causes the at least a flexible part to deflect outwardly with further distal displacement of the piston rod causing the intermediate part to wholly pass through the first opening with the at least a flexible part returning towards the at rest state, engagement of the at least a flexible part with a surrounding element under force of movement towards the at rest state generating a sound.

Abstract: An implant delivery syringe includes a barrel, a plunger assembly, and a barrel adapter. A barrel adapter mountable to a syringe barrel includes a barrel tip, needle retraction mechanism, needle assembly and stylet slidably disposed within the needle lumen. The needle retraction mechanism includes a biasing member, actuable locking arrangement and locking mechanism. When the actuable locking arrangement is actuated, the biasing member causes the needle to axially translate over the stylet during retraction to cause delivery of an implant to a target location. The stylet may be retracted following delivery. Methods of assembling, manufacturing, and using are also provided.

Abstract: The invention is a single use syringe having an integrated mechanism to prevent its reuse, by manual intentional destruction after use, by an easy move. This prevents the reuse of syringes which may result in disease transmission if it is contaminated. It prevents auto destruction at an unwanted period so that it can be used for multiple purposes like blood aspiration and injection for a single patient and then dispose it as the medical staff stop attending that individual, thus saving valuable resources and generating less plastic waste. The manufacturing process is simple and brings not much added cost or special training for operation. The step for destruction is simple and quick without the aid of any special equipment, additional staff or electricity.

Abstract: A safety syringe includes a barrel, a plunger, and a needle hub. The barrel is extended axially and includes a first tube portion, a second tube portion extended from an end of the first tube portion, and a first folded ring flexibly branched and formed on an inner side of the first tube portion and disposed around the axis, such that after the first folded ring is unfolded, the first folded ring is bounded and extended from the first tube portion towards the second tube portion, and includes a movable first flexible portion. The plunger includes a rod extended along the axis. The needle hub is detachably installed in second tube portion. The plunger can be moved to an injecting position, a limit position, and a disposal position with respect to the needle hub.

Abstract: The present invention provides a disposable syringe and a push rod for use in a disposable syringe. The push rod comprises a proximal end, a distal end and an axis extending through the proximal end and the distal end. The distal end of the push rod is provided with a snap-fitting mechanism and a stop flange located at a proximal side of the snap-fitting mechanism. The stop flange comprises a main body portion formed about an axis of the push rod and a plurality of finger-like portions extending from the main body portion in a direction away from the axis of the push rod. According to the present invention, a smaller push force continues to be applied to the push rod upon completion of the injection, thereby achieving an additional stroke needed when the distal end of the push rod snap-fits with the needle seat and meanwhile lessening the patient's pains.

Abstract: A drug delivery device for setting and dispensing a dose of a drug is presented having a support body having a first end defining a first opening and a second end defining a second opening and a centered outer indicator ring. A syringe barrel sealed by a stopper is slidably disposed therein along an axial direction and adapted to have an integrated needle or to be coupled with a needle assembly, wherein the syringe barrel is positioned within the support body. A needle shield is adapted to be coupled to one of the ends of the support body and slidably disposed thereon. An outer body is adapted to be coupled to the other end of the support body and slidably disposed thereon, wherein the outer indicator ring limits the movement of the outer body as well as of the needle shield.

Abstract: A safety intravenous cannula and catheter device is disclosed. The device permits easy insertion of a cannula made of a biocompatible material into the vein with a guide needle and withdrawal of the guide needle into a safety chamber with an in- built locking mechanism with completely prevents removal and/reuse of the needle. The needle before insertion is protected by a biocompatible sheath which when inserted into the vein and after withdrawal of the needle acts as catheter. Similarly, after withdrawal the needle is locked inside a safety chamber in such a manner that at no time does the user come into contact with the needle or in any danger of accidental injury.

Abstract: The technical problem of the present invention to provide a medical device, which exhibits an increased safety of the device and facilitates a safe use is solved by medical device for delivering at least one drug agent, comprising a sensor, a control unit and an attachable dispense assembly, wherein the sensor is configured to detect attachment of the dispense assembly to the medical device, wherein the control unit is configured to determine at least based on a signal from the sensor whether the end of life of the dispense assembly is reached and wherein the medical device is configured to indicate the end of life of the dispense assembly. The technical problem is further solved by a method according to the invention.

Abstract: The present invention disclosed a retractable self-destroying safety syringe with replaceable needle including a barrel body, a needle base body (3) disposed in a barrel neck (2) at an end of the barrel body (1), an elastic buffering engaging mechanism formed between the barrel neck (2) and the needle base body (3). An asymmetrical elastic retracting locking member having an elastic function is disposed at an end of a plunger, with which an internal sleeved retracting locking member of the needle base body can be interlocked by the elastic function. After being retracted into the barrel body (1), the needle base body is deflected to one side under an asymmetric force, and the needle therefore inclines in a direction nearly a 45 degree angle to one side of the inner wall of the barrel body (1) and is blocked by the barrel neck of the barrel body, so that the needle and the needle base could not be pushed out of the barrel neck again and self-destruction of the syringe is truly achieved.

Abstract: A liquid administration device includes: a cylindrical body filled with liquid; a needle tube configured to communicate or be communicable with the cylindrical body at its tip side, and to have a sharp needle tip; a gasket configured to slide within the cylindrical body; an operation member configured to to discharge the liquid by pressing the gasket toward the tip direction; a cover member configured to be capable of moving to a first position, in which at least the needle tip is covered, to a second position, in which the needle tip is exposed, and to a third position, in which at least the needle tip is re-covered; and a cover member that can move from the first position to the second position to a third position to re-cover the needle tip.

Abstract: Protective devices for injection needles or infusion needles that include a needle holder at a proximal end of the needle, on whose shaft a protective element for the needle tip can be positioned and moved, are herein disclosed. The protective element is configured to block the needle tip following an injection to prevent accidental contact therewith. The protective element may be positioned on the shaft in a ready to use position inside a grip part or middle retaining portion, which is also used to activate the protective element over the needle following the injection.

Abstract: An injection device has a main drive module which can be screwed into the back of a syringe housing to prepare the injector ready for use. The drive module has a firing button and a drive plunger released for forward movement by pressing the firing button. The syringe housing slideably receives a syringe holder whose forward movement is initially prevented by internally directed barbs on a cylindrical latching sleeve. The latching sleeve is acted upon by a release ring on the drive module such that as the drive module is screwed onto the syringe housing, the release ring splays the cylindrical shell to release the syringe carrier for forward movement. The barbs also act as a latch to capture the syringe carrier in its rearward position when the drive module is unscrewed from the syringe housing, which returns the barbs to their initial position before the syringe holder returns to its initial position.

Abstract: A portal access assembly includes an inserter that has a needle, a cap moveable along the length of the needle and an infuser having a cannula through which the needle extends. A safety mechanism inside the cap allows the needle to be moved relative to the cap so long as the shaft of the needle biases against an edge of one of the legs of the mechanism. After the cannula is properly positioned in the implanted port to establish a fluid path between the port and the infuser, the needle is removed by being pulled upwards until it no longer biases the one leg of the mechanism. At which time the safety mechanism fixedly captures the needle inside the cap to prevent the contaminated tip of the needle from being exposed to the environment. At the same time, the cap is detached from the infuser.

Abstract: A skin insertion mechanism of a needle fixedly positioned in a needle holder with connective means to an injection or analysis system has a skin attachment plate coated with an adhesive layer and a spacer mechanism keeping in the ready-to-use position the skin attachment plate spaced away from the needle support covering the needle. Subcutaneous insertion of the needle is effected by attachment with the adhesive layer to the skin and releasing the spacer mechanism by applying a pre-set trigger point pressure against the skin.