Abstract: A Hypodermic Needle Safety Guard intended for sharps prevention and safer hypodermic needle use during all stages of an injection process. The Safety Guard may include two symmetrically positioned multi-featured arms that include spring tension, multiple hinges and needle locks. These arms may connect a proximal Luer body and a distal alignment tip thereby enabling the guard to open, close and lock on a needle when manual pressure is applied. The Guard position during hypodermic needle use tends to prevent sharps injury by adjusting the exposure of the Needle tip.

Abstract: An apparatus includes a catheter, an introducer, and an actuator. A distal end portion of the introducer is configured to be coupled to a peripheral intravenous line. The introducer defines an inner volume having a first portion that defines an axis parallel to and offset from an axis defined by a second portion. A first portion of the actuator is movably disposed in the first portion of the inner volume. A second portion of the actuator is movably disposed in the second portion of the inner volume and coupled to the catheter movably disposed in the second portion of the inner volume. The actuator moves the catheter between a first position, in which the catheter is disposed within the introducer, and a second position, in which at least a portion of the catheter is disposed within the peripheral intravenous line.

Abstract: A biopsy device comprises a body, a needle, a cutter, and a tissue sample holder. The tissue sample holder comprises an outer cup and a cap. A tray retains severed tissue samples from a biopsy procedure. In some versions, the tray is selectively detachable from the cap in a one-handed operation by the user. The tray may be ejected into a sample container, such as a formalin cup. The cap may include a threaded portion that is configured to engage a complementary threaded portion of a sample container to seal the sample container once the tissue samples have been transferred to the sample container from the tissue sample holder of the biopsy device. One or more ports may be provided in the cap to manage excess fluid within the outer cup of the tissue sample holder, and/or to provide integrated access for a marker delivery device.

Abstract: A catheter assembly comprises: a catheter; a catheter hub fixed to a proximal end portion of the catheter; an inner needle disposed inside the catheter; and a housing; wherein a distal end of the housing comprises a portion configured to support the inner needle via the catheter; wherein, when the catheter assembly is in an initial state in which a distal end of the inner needle protrudes from a distal end of the catheter, the housing accommodates the catheter hub; and wherein the catheter hub is configured to rotate with respect to the inner needle and the housing when accommodated inside the housing.

Abstract: A catheter system may include a catheter hub, a septum disposed within the catheter hub, a catheter tube extending from the catheter hub, a needle hub, and an introducer needle secured within the needle hub. The catheter hub may include a push tab and one or more ribs, which may extend outwardly from an upper surface of the catheter hub. The ribs may be shorter in height than the push tab and/or may be generally parallel to the push tab. The introducer needle may include a flashback notch. In response to insertion of the introducer needle into vasculature, blood may flow into the introducer needle, through the flashback notch, and into a flashback chamber disposed between the septum and the catheter tube. The flashback chamber may be disposed distal to the push tab and the ribs, which may improve visualization of the flashback chamber by a user.

Abstract: The present disclosure provides for a safety catheter assembly comprising a needle hub, a catheter hub, a tip protector housing. Various embodiments can comprises a push-off tab extending radially from the tip protector housing or a portion thereof, and/or structure can be added or removed to affect compliance between a catheter assembly and a catheter insertion device.

Abstract: The invention provides device for needle biopsy having a novel delivery handle system for interchangeably delivering needles of various sizes to a biopsy site. The delivery handle system is adjustable in length and includes a proximal slideably disposed over a middle handle member, the middle handle member is slideably disposed over a distal handle member. The proximal handle member includes an inner hub housing component configured to interchangeably receive a needle subassembly that can be inserting into and withdrawn from the proximal handle member. The needle subassembly includes a needle of a plurality of different sizes, a needle luer, a needle hub coupled to a proximal end portion of the needle, and a needle protector subassembly. The needle protector subassembly includes a needle protection hub configured to receive the distal end of a needle.

Abstract: The invention relates to an insertion device (110) for inserting an analyte sensor (114) into a body tissue. The insertion device (110) comprises an insertion needle holder (120) and a drive mechanism (124) for driving the insertion needle holder (120) in a longitudinal direction (126). The drive mechanism (124) comprises at least one actuator (132) for actuating the drive mechanism (124). The drive mechanism (124) comprises a rotor (142) adapted to transform an actuation motion of the actuator (132) into a motion of the insertion needle holder (120) in the longitudinal direction (126). The insertion device (110) further comprises at least one safety lock (164). The safety lock (164), in a locked position, is adapted to at least partially block a rotation of the rotor (142). In an unlocked position, the safety lock (164) is adapted to permit the rotation of the rotor (142).

Abstract: A catheter assembly may include a cannula. The cannula may include a distal tip, an elongated tubular shaft, and an inner lumen formed by the elongated tubular shaft. A first portion of the elongated tubular shaft may have a first outer diameter. The first portion may be proximate the distal tip. A second portion of the elongated tubular shaft may have a second outer diameter. The second outer diameter may be greater than the first outer diameter. The catheter assembly may also include a catheter adapter, which may include a catheter and a catheter hub. The second portion of the elongated tubular shaft may be at least partially disposed in the catheter hub.

Abstract: A two-stage infusion set inserter system is disclosed. The inserter system includes an inserter assembly including a housing including a rotatable button assembly comprising ramps and and tab indents and a non-rotatable portion of housing, a sliding component comprising sliding component tabs, a needle carrier connected to an introduction needle, the needle carrier slidably movable from a starting position to an injection position and then to a second ending position, a sliding component spring, and a needle spring, wherein the rotatable button assembly rotates from a locked to an unlocked position, wherein when force is applied onto the rotatable button assembly, the sliding component and needle carrier are forced downward by the sliding component spring, and wherein when the needle carrier reaches the injection position, the needle spring forces the needle carrier upward towards the second ending position.

Abstract: A medical safety needle is comprised of a needle body having a needlepoint, a covering body having a detent portion slidable on the needle body to catch the needlepoint so as to cover the needlepoint, and a resilient cantilever supporting the detent portion, a sleeve following the covering body to cover a side face of the needle body, a collar portion slidably fitting on the covering body, which is configured to get in contact with the cantilever to press the cantilever radially inwardly, and a housing being formed in a unitary body with the collar portion or having an end face on which the collar portion is capable of being seated, the housing being configured to carry the covering body from a first position to have the needlepoint exposed to a second position to have the needlepoint covered by the covering body.

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 at least partially encloses the piercing means and the syringe body, and an inner element which is at least arranged at least in sections inside the sleeve element and surrounds the piercing means. Said safety device is characterised in that the inner element comprises a rim section and a piercing means protection section surrounding the piercing means. Said rim section can be arranged on a distal end of the syringe body, the safety device is secured to the syringe body, and the piercing means protection section can be removed from the rim section before using the syringe.

Abstract: A blood collection tube holder embodying two coaxially alignable needles, the first needle being a forwardly facing venipuncture needle and the second needle being a rearwardly facing fluid discharge needle. The first and second needles are satisfactorily supported by a frontal attachment and body, respectively, that are disposed in relative sliding engagement along an interface that is transverse to the first and second needle and that extends at least from the second needle to an opening into a needle retraction chamber that projects rearwardly from the body. The subject device is configured to receive and support a conventional blood collection tube of the type used to collect blood samples.

Abstract: A catheter assembly including a catheter; a catheter hub fixed to a proximal end portion of the catheter; an inner needle disposed inside the catheter; and a housing supporting the inner needle, the housing accommodating the catheter hub when in an initial state in which a distal end of the inner needle is protruding from a distal end of the catheter. The catheter hub is configured to rotate with respect to the inner needle and the housing when accommodated inside the housing.

Abstract: A safety needle system includes a safety mechanism for a needle assembly, such as a Huber needle. A main body has a channel having a proximal end to encompass tubing and a distal end for positioning proximate a needle. The main body further has a first hinge mechanism and a first latching mechanism. A movable cover has needle receptacle, a second hinge mechanism connected with the first hinge mechanism of the main body, and a biasing member for pivoting movable cover about the first and second hinge mechanisms relative to the main body. The movable cover has a second latching mechanism to latch with the first latching mechanism in a closed position, in which the safety mechanism can be undocked from the needle and slid away from the needle along the tubing. The movable cover has a release mechanism to allow pivoting of the movable cover about the hinge mechanisms such that the needle receptacle of the movable cover at least partially receives the needle of the needle assembly in an open, locked position.

Abstract: A medical device, such as a Huber-type device, includes a structure that enhances operator safety by reducing the likelihood that a needle will accidentally injure an operator. In one embodiment, the device includes a collapsible structure that can move from a use position to a non-use position. The device includes first and second wing portions and a channel for covering the needle as it is extracted from the patient. The structure enables the operator to leverage applied pressure for a smooth removal of the needle into the device for safe disposal.

Abstract: This invention relates to a modular purification system having a disposable sump assembly and an improved flow distribution plate. The system is readily adaptable to a variety of configurations without the need for repiping or replumbing of the installation, and lends itself to the use of multiple purification techniques.

Abstract: A cannula and needle assembly configured to first have the needle assembly create an opening in the skin of a person or animal and to then insert the cannula through the needle into the person or animal by way of the opening created by the needle. The assembly also includes structure to yieldably maintain the needle assembly in a docked position.

Abstract: An infusion set has an adhesively secured main hub, and a slidable top cover, needle hub and angled or cantilevered needle that can be used for performing an intradermal needle insertion precisely targeting the upper 3 mm of skin surface, for example, one that substantially duplicates the Mantoux insertion technique, for injecting into the intradermal layers of skin, while maintaining a degree of comfort to the user. By sliding the top cover, the cantilevered needle is loaded and released or the angled needle is slid into an insertion site, while flexible arms and adhesive are used to stretch and/or flatten a skin surface, or otherwise create skin tension, at the insertion site.

Abstract: A needle retraction apparatus comprising a body having a forwardly projecting needle, a needle retraction mechanism seated inside the body and biasing the needle rearwardly relative to the body, a slide member attachable to the body and having an opening communicating with a needle retraction cavity projecting away from the body, and an actuator rotatable relative to the slide member to reposition the slide member from a first position preventing needle retraction to a second position permitting needle retraction. An IV catheter introducer comprising the subject needle retraction apparatus is also disclosed.

Abstract: An infusion set adapted to be secured to a skin surface includes a fixed base member and a movable slide member. The fixed base member is connectable to the skin surface. The movable slide member has a needle or cannula connected thereto and is movable relative to the fixed base member. The movable slide member is movable from a first position in which the needle or cannula is not exposed externally of the fixed base member to a second position in which the needle or cannula is exposed externally of the fixed base member. The movable slide member is locked to the fixed base member in the second position.

Abstract: A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.

Abstract: An insertion device with an underside for placing on the skin of a patient, which has a recess for an insertion needle. The insertion device has means for forming a skin surface rising like a step or slope and facing towards the recess, preferably bearing on the recess. The means for forming the step or slope may include first and second pressure areas for pressing the skin with the recess for the needle located between the first and second pressure areas. The device may be configured whereby a downwardly extending cutting plane, in which the insertion needle lies, intersects the first pressure area in a first line and the second pressure area in a second line, and wherein the first line in the vicinity of the recess extends at a greater height than the second line. At least one of the two pressure areas may be a strip.

Abstract: There are disclosed devices and methods for protecting a user from a sharp tip of a medical needle. In an embodiment, a device includes a central body portion, a medical needle having a sharp tip, a pair of wings in attachment to the central body portion, and a mechanical fastener disposed on at least one of the wings, the mechanical fastener configured to selectively attach the wings together with the medical needle positioned between the wings so as to protect a user from the sharp tip of the medical needle. In another embodiment, a method includes withdrawing a sharp tip of a medical needle from a patient, closing a pair of wings with the medical needle positioned between the wings, and fastening the wings together with the medical needle positioned between the wings so as to protect a user from the sharp tip of the medical needle.

Abstract: The present invention generally provides methods and devices for removing fluid from a surgical instrument. Surgical access devices and seal systems are generally provided having one or more valves or seal assemblies to create a closed system between the outside environment and the environment in which the surgical access device is being inserted. In one embodiment, a seal assembly is provided and can include a seal having an opening configured to receive a surgical instrument therethrough and a fluid remover in the form of a sorbent element, a scraper element, a wicking element, or any combination thereof can be associated with the seal and configured to remove fluid from the opening and/or a surgical instrument.

Abstract: The invention relates to a needle protector assembly (10) comprising a needle defining an axial direction and a protective cover for the needle. The needle is attached to a needle hub which is provided with wings on opposite sides thereof and which can be moved relative to the protective cover between a distal position in which at least a tip of the needle protrudes from the protective cover, and a proximal position in which the needle is fully received in the protective cover. The protective cover comprises first (26) and second parts (28) which together form an elongate housing along which the needle hub can move between the distal and proximal positions, wherein the first and second parts define elongate slots on opposite sides of the housing through which the wings (16) protrude.

Abstract: A sample liquid supply device includes a container tip into which the sample liquid is introduced, a hollow needle provided at one end of the container tip such that a hollow part thereof communicates with inside of the container tip, and a sealing member that covers an opening from which the sample liquid is introduced, wherein the sealing member has a puncture-sealing property achieved by elastic deformation.

Abstract: A safety IV catheter assembly is disclosed which includes a catheter assembly, a needle assembly and a needle guard assembly. The needle guard assembly includes a needle guard, a biasing member and a bushing. The bushing is slidably positioned about the needle and includes an inner diameter which is smaller than an enlarged diameter portion of the needle such that the needle cannot be withdrawn through the bore of the bushing.

Abstract: A needle assembly adapted for fluid communication with a cartridge containing a substance to be delivered to a subject, the needle assembly characterized by a biasing device (70) arranged to apply a biasing force on a needle (28, 116) to cause the needle (28, 116) to protrude outwards of a housing (30, 112) to pierce the subject, and biasing device release apparatus (60) including a biasing device arrestor (62) that initially blocks movement of the biasing device (70) and which releases the biasing device (70) when the safety latch (32, 122) moves to a position that permits moving the needle holder (26, 118) to cause the needle (28, 116) to protrude outwards of the housing (30, 112).

Abstract: The invention pertains to an applicator (1) for inserting an implant, in particular a rod-like implant (2) containing an active substance, under the skin of a human or animal, comprising a housing (3), a cannula (6) extending from the housing (3), and a handle (15) for grasping and maneuvering the applicator (1) and the cannula (6) during insertion of an implant (2). In accordance with the invention, the handle (15) extends above at least part of the length of the cannula (6). Such a handle facilitates insertion of the cannula and/or accurate positioning of the implant.

Abstract: A needle assembly for a medical device comprising a needle cannula which is mounted in a hub connectable to a medical device, and which needle assembly comprises releasable locking means which co-operates with the connection means of the hub such that the needle cap is locked to the hub when the releasable locking means is not released. Once the locking means is released by activation of the connection means, the needle cap is unlocked from the hub. The activation of the locking means is preferably done automatically when the needle assembly is attached to the medical device.

Abstract: A method of using a safety enclosure for a needle, the needle including an aft end and a fore end together forming a right angle, the fore end including a sharp outer end. The method includes providing a safety enclosure including a needle housing and a panel unit, the needle housing having a finger pad, orienting the safety enclosure in a desired location for insertion of the needle, and applying pressure to the finger pad sufficient to cause penetration of the needle at the desired location and to move the panel unit to the installation position.

Abstract: An infusion pump system is described that increases patient comfort and convenience. The infusion pump system includes an infusion site interface that is releasably connected to an infusion pump body, and has no tubing associated between the infusion site interface and the pump body. The infusion pump body may include a carrier frame that may be adhered to the skin of a user.

Abstract: The invention relates to a system for injecting a liquid into a body, comprising an implantable chamber disposed under the skin and an injection device including: a base bearing an injection needle having a free end that is intended to be inserted into the chamber; an injection conduit connected to the needle; means for extracting the needle; means that can be actuated to generate excess pressure in the injection conduit; synchronization means between the extraction means and the generation means for actuating the generation means during a needle extraction phase. The synchronization means can essentially only actuate the generation means when the free end of the needle is located in the chamber during the needle extraction phase.

Abstract: The invention presented is a needle system to access a subcutaneous port primarily for the administration of chemotherapy, designed to protect the health care worker from inadvertent needle injury by isolation of the needle tip within base and tower components. A rotating collar is designed to keep the needle immobile until access of the port is desired when it can be rotated to align a cut out with a corresponding cut out of the tower that houses the needle for advancement of the needle downward into the port. On retraction, the collar can be rotated, locking the needle back into a retracted position within the tower.

Abstract: A safety enclosure for a Huber needle includes a needle housing and a panel unit. The panel unit includes a series of planar panels assembled in an enclosing arrangement defining an enclosed area and is movable between an installation position where the sharp outer end of the Huber needle projects from the panel unit and a safety position where the sharp outer end is covered by the panels. The Huber needle has an aft end and a fore end connected by a bend with the fore end including a sharp outer end.

Abstract: An infusion pump system is described that increases patient comfort and convenience. The infusion pump system includes an infusion site interface that is releasably connected to an infusion pump body, and has no tubing associated between the infusion site interface and the pump body. The infusion pump body may include a carrier frame that may be adhered to the skin of a user.

Abstract: An infusion pump system is described that increases patient comfort and convenience. The infusion pump system includes an infusion site interface that is releasably connected to an infusion pump body, and has no tubing associated between the infusion site interface and the pump body. The infusion pump body may include a carrier frame that may be adhered to the skin of a user.

Abstract: An infusion pump system is described that increases patient comfort and convenience. The infusion pump system includes an infusion site interface that is releasably connected to an infusion pump body, and has no tubing associated between the infusion site interface and the pump body. The infusion pump body may include a carrier frame that may be adhered to the skin of a user.

Abstract: An I.V. catheter assembly and needle safety device are disclosed which allow for the safe removal of a needle from a catheter assembly. The safety device includes a locking assembly which includes lock housing a rotatable locking member and a locking clip. The needle and the locking member are configured such that withdrawal of the needle from the catheter assembly effects rotation of the locking member. The locking clip is positioned and configured to obstruct rotation of the locking member after the needle has been retracted within the housing to obstruct re-advancement of the needle.

Abstract: A closable male luer connector is provided in which an inner portion within the spigot of the connector is movable from a sealing position to an open position on connection of the connector to a female luer connector wherein the movement of the inner portion may be caused by, for example, action of the female connector on a projecting arm or a screw thread arrangement.

Abstract: The present invention generally provides methods and devices for removing fluid from a surgical instrument. Surgical access devices and seal systems are generally provided having one or more valves or seal assemblies to create a closed system between the outside environment and the environment in which the surgical access device is being inserted. In one embodiment, a seal assembly is provided and can include a seal having an opening configured to receive a surgical instrument therethrough and a fluid remover in the form of an absorbent element, a scraper element, a wicking element, or any combination thereof can be associated with the seal and configured to remove fluid from the opening and/or a surgical instrument.

Abstract: A catheter for introduction and removal of fluids from a body and tunneling device therefor, the catheter has a body having a first conduit for removing fluid from the body and a second conduit for delivering fluid to the body wherein at least a part of each of the conduits is integrally formed within a first end of the body of the catheter and extends along side one another. The first conduit extends beyond the second conduit and forms a terminal point of the first end and defines a first opening thereat and the second conduit extends to a point short of the terminal point defining a second opening. A bumper portion is adjacent the second opening extending toward the terminal point. Another part of each the first and the second conduits are disjoined and form part of a second Y-shaped end. The tunneling device has a channel to removably receive the catheter.

Abstract: A medical device for placement of regional anesthesia catheters. The device comprises a hollow shaft needle, a plunger attached to the posterior end of the needle, a housing dimensioned so that plunger can slide inside the housing with friction, a regional anesthesia catheter preloaded inside the needle, a protective cover sheath covering the catheter, and a catheter adaptor attached to posterior end of the sheath and the catheter. The medical device allows a practitioner to quickly and effectively place a regional anesthesia catheter inside an organism without the use of an assistant, and with minimal risk of contaminating the catheter before it enters the organism's body. At the end, the needle is withdrawn inside the housing and disposed.

Abstract: An indwelling needle assembly, including an inner needle having a sharp needle point at a distal end thereof; an inner needle hub which is fixed to a proximal portion of the inner needle and which has a proximal end face; a hollow outer needle into which the inner needle is inserted; and an outer needle hub fixed to a proximal portion of the outer needle, the inner needle is adhered and fixed to the inner needle hub with an adhesive at a proximal portion thereof, and the inner needle hub is provided with a projected part formed by projecting the adhesive toward a proximal side relative to the proximal end face.

Abstract: A needle assembly includes a mounting structure and a needle mounted on the mounting structure and extending outwardly from the mounting structure. The needle has a longitudinal axis, a sharp end and a central axial passageway. A safety shield is associated with the needle and includes a tubular housing having distal and proximal ends. The distal end of the housing has a funnel-shaped surface. A reset key is configured to engage the distal end of the housing. The reset key includes a support. A shaft extending from the support is adapted for inserting into the distal end the housing. The funnel-shaped surface guides the shaft into the housing to register the reset key with the safety shield.

Abstract: A protector is attached for use to a needle body having a main needle body and an enlarged-diameter section having an outer diameter greater than that of the main needle body. The protector includes a platelike protector body made of a metal material. The protector body includes a first section formed with a first hole adapted to receive the needle body when the needle body is passed therethrough, a second section formed with a second hole, and a third section adapted to connect the first section and the second section. The second hole of the second section is provided with a tubular portion that permits the main needle body to pass therethrough, but prohibits the enlarged-diameter section from passing through the tubular portion. In a state in which the protector covers the needle tip, the tubular portion comes into abutment against the enlarged-diameter section, thus prohibiting the needle body from moving toward the proximal side.

Abstract: A safety enclosure for a Huber needle includes a needle housing and a panel unit. The panel unit includes a series of planar panels assembled in an enclosing arrangement defining an enclosed area and is movable between an installation position where the sharp outer end of the Huber needle projects from the panel unit and a safety position where the sharp outer end is covered by the panels. The Huber needle has an aft end and a fore end connected by a bend with the fore end including a sharp outer end.

Abstract: A protector comprising an inner tube, a lid connected to an upper opening of the inner tube through a hinge, and an outer tube for holding the inner tube in an inner cavity part of the outer tube. A blood collecting needle to which a tube is connected is stored in the inner tube. The inner tube comprises an annular seat face which seats on the base end part of a hub formed integrally with the blood collecting needle when the blood collecting needle moves downward. An operation lever extending downward is installed at the side of the lid, and an end part of the operation lever is slightly projected outward. When the blood collecting needle is moved, the inner tube is pulled integrally with the tube by the annular seat face to be slid relative to the outer tube until the end part abuts on the lower end part of an operation hole. Then, the lid is closed and the blood collecting needle is stored in the inner tube.

Abstract: A needle protection device detachably fixed to an injection appliance includes a needle, a needle holder from which a needle injection section of the needle projects distally and a needle connection section of the needle projects proximally, a distal needle protection element connected to the needle holder movable in the distal direction from a release position to a protection position and arranged behind the needle injection section in the release position and overlapping the needle injection section and distal end of the injection needle in the protection position, a proximal needle protection element connected to the needle holder movable from a release position and arranged behind the needle connection section into a protection position and overlapping the needle connection section and proximal end of the injection needle, and a blocking device which blocks movement of the proximal needle protection element from the protection position into the release position.