Abstract: A drug delivery device comprises a cap releasably secured to a main body of the drug delivery device and a needle assembly retained within the cap. The drug deliver device also includes a pre-stressed biasing element disposed between the cap and the needle assembly and configured to bias the needle assembly in a distal direction with respect to the drug delivery device while the cap is secured to the main body. The drug delivery device further comprises one or more locking elements each having a locked position and an unlocked position. In the locked position, the locking elements prevent the needle assembly from engaging with a cartridge retained within the main body. In an initial position, the cap is configured to retain the locking elements in the locked position. In an intermediate position, the cap is configured to release the locking elements to allow the needle assembly to engage with the cartridge.

Abstract: A medical device for percutaneous or venous access for the purposes of administering a fluid to a patient or sampling from one is disclosed. The device includes a cannula holder that has a part or portion of cross-section which is reduced or different from its distal end and proximal end. The part or portion of reduced or different cross-section allows the cannula holder to deform within the body of the device when activating means are activated to separate the cannula holder from an immobilising member allowing the cannula holder to move in the body of the device and re-enter and disappear within such body of the cannula.

Abstract: A catheter insertion device includes a hollow needle attached to a needle base. A compression spring mechanically biases the needle base away from a plunger. A catheter is configured to be contactable by the plunger when the plunger moves in a forward direction. An expandable chamber is in fluidic and/or pneumatic communication with the hollow needle. The plunger inserts the catheter when a vacuum formed in the expandable chamber by the compression spring pushing the plunger away from the needle base is released by a fluid and/or a gas entering the hollow needle at a distal skin-piercing end as it punctures a vein or artery. The plunger is moved from a stored position to the armed position by rotating a button which overcomes any tendency for the plunger to stick in place during storage. The needle can be retracted by the same compression spring after the catheter is inserted.

Abstract: A connector is connectable to a medical device that includes a female connector portion. The connector includes: a main body member including: a cylinder portion that is insertable into the female connector portion, and a lock portion configured to, upon insertion of the cylinder portion into the female connector portion, pass over part of the medical device and then move in a predetermined locking direction to lock the medical device; and a lock member that is movable with respect to the main body member. When the main body member is in a state in which the lock portion locks the medical device, the lock member is moveable to a lock position at which the lock member limits movement of the lock portion in a predetermined unlocking direction.

Abstract: The present invention relates to a drive mechanism for use with a medicament delivery device, comprising a plunger rod (68), a drive spring (72) operably arranged to the plunger rod, an actuator (52) comprising a holding member (60) releasably engaged to the plunger rod (68) for holding said plunger rod (68) with said drive spring (72) in a tensioned state, a rotator (38) operably connected and movable relative to said actuator (52) and configured to interact with said holding member for holding said holding member in engagement with the plunger rod, an activator (30) operably connected to said rotator (38). The invention is characterized in that the activator (30) is configured to rotate and subsequently linearly displace the rotator (38) in relation to the actuator (52) such that said holding member (60) is released from the plunger rod (68).

Abstract: Some embodiments of a medical device anchor system include an anchor device that secures a medical instrument (such as a catheter or the like) in place relative to a skin penetration point using subcutaneous anchors.

Abstract: A telescoping catheter including an elongated tubular member having a proximal end, a distal end, and a passageway extending between the proximal end and the distal end. The tubular member includes a first tubular segment and a second tubular segment. The first tubular segment and the second tubular segment are slidable relative to one another to vary a length of the tubular member. The first tubular segment includes a first connector mateable with a second connector of the second tubular segment to selectively maintain the first and second tubular segments in an extended position. The second tubular segment includes a second proximal end that is mateable with a handle.

Abstract: An introducer needle may include a proximal end, a distal tip, and a needle lumen extending therebetween. The introducer needle may include a wall defining the needle lumen, a first notch formed through the wall, and a second notch formed through the wall. A catheter system may include a catheter adapter, a catheter extending distally from the distal end of the catheter adapter, a flash chamber coupled to the introducer needle, and the introducer needle, which may extend through the catheter. The first and second notches and the flash chamber may facilitate pressure-driven blood flow into the catheter for improved flashback and detection of transfixation when the catheter is primed prior to insertion into vasculature of a patient or otherwise.

Abstract: A medical connector assembly for establishing a fluid connection between a first medical device and a second medical device includes a multi-use connector and a plurality of single-use connectors connected in series. The multi-use connector has a proximal end opposite a distal end along a longitudinal length thereof. The plurality of single-use connectors each have a proximal end opposite a distal end along a longitudinal length thereof. The distal end of the multi-use connector is releasably connected to the proximal end of a first of the serially-connected single-use connectors. When a second of the serially-connected single-use connectors is disconnected from the first single-use connector, the first single-use connector remains connected to the multi-use medical connector as a sterility retaining cover.

Abstract: A transfusion speed regulator, a transfusion monitoring system and an operation method of the transfusion monitoring system are disclosed. The transfusion speed regulator includes a housing, a lead rail, an actuator and a regulating roller. The housing includes a bottom plate; the lead rail is on the housing and is not parallel to the bottom plate; the regulating roller is configured to be moved along the lead rail to regulate a transfusion speed; and the actuator is configured to drive the regulating roller to move.

Abstract: A needle housing having a distal end which is removably connectable to a source of injectable fluid and a proximal end for contacting a patient. The needle housing comprises (a) a hollow needle having a proximal end for insertion into body tissue of the patient, and (b) a chamber having an open proximal end, the chamber surrounding at least part of the needle and extending proximally beyond the proximal end of the needle to the open proximal end. The open proximal end of the chamber is deformable and moveable relative to the needle from a position in which the chamber extends proximally beyond the proximal end of the needle to a position in which the proximal end of the needle extends proximally through the open proximal end of the chamber.

Abstract: Stabilizers for intraosseous devices, such as, for example, stabilizers that may be coupled to an intraosseous device (e.g., a device including an intraosseous needle) while a portion of the device extends into a patient's bone and/or while the device is coupled to a fluid source (e.g., FV bag, syringe, etc.).

Abstract: In some aspects, a dialysis machine support assembly includes a platform configured to support a dialysis machine and a drive assembly configured to move the platform vertically.

Abstract: A catheter tip that provides longitudinal flexibility, pushability and radial rigidity thereby improving deliverability is provided. The catheter tip includes a spring-like element to provide longitudinal flexibility and pushability to the catheter tip. The spring-like element may also provide radial support to the distal edge of the catheter tip. Alternatively, a radially rigid distal end may also be included distal of the spring-like element. The apparatus may be used with any interventional catheter system, but is particularly suitable for use with balloon-expandable stent systems and balloon-angioplasty systems, where flexibility of the catheter tip and minimal flaring of the distal edge of the catheter tip is desirable.

Abstract: An occlusion assembly for compressing a pair of collapsible tubes comprises a frame comprising a tubing guide configured for positioning the collapsible tube. The occlusion assembly also comprises a tubing occluder mounted to the frame with an occluding member constructed and positioned to controllably occlude or release occlusion of the collapsible tube. A door mounted to the frame is positioned to cover at least a portion of the collapsible tube and tubing occluder when closed and provide user access when open. The assembly includes a retainer mechanism engaged by the door when the door is closed to permit operation of the tubing occluder when the door is closed and retain the tubing occluder in a non-occluding configuration when the door is opened.

Abstract: A needleless injector includes a cap, an injection system, a body, a gas generator, and a percussion device. The body is covered by the cap and is mounted to slide relative to the cap. The percussion device includes a striker that is slidingly mounted along a sliding axis between a rest position and a percussion position and a lock mechanism. The lock mechanism includes a lug and a retention tab. The lug projects from a peripheral face of the striker along an axis that is perpendicular to the sliding axis and has a first support ramp. The retention tab is attached to the cap, and has a second support ramp. The ramps are configured to move the retention tab radially when pushed by the striker from a retaining position to a release position and the retention tab is moved aside to release the striker.

Abstract: A method and apparatus for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump is provided. The reservoir, a base and a cap are connected to form an integrated unit that is capable of being inserted and secured in an infusion pump housing. The cap and the infusion pump are each provided with at least one sensor or at least one detectable feature, arranged to interact with at least one corresponding detectable feature or sensor on the other of the cap and infusion pump device, to detect one or more of the presence, position or other characteristic of the cap when the cap is aligned or coupled with the infusion pump housing. The detectable feature and sensor may be magnetic, RF, mechanical, optical or any combination.

Abstract: Devices and methods for balloon delivery of rapamycin and other hydrophobic compounds to the wall of blood vessels. Balloon catheters, such as those used for balloon angioplasty, are modified with the addition of a reservoir of dry micelles. The micelle preparation is reconstituted and the micelles are mobilized when the aqueous solution used to inflate the balloons is injected into the catheter. The micelles are infused into tissue surrounding the balloon when pressurized fluid within the balloon leaks through the wall of the balloon.

Abstract: A control system and method are provided for control of a steerable catheter, the catheter including at least two control wires, a distal end of each of the control wires being coupled to the catheter at a distal region thereof, the control system comprising: a housing coupled to the catheter; a slide assembly positioned within the housing and operable to translate linearly therein; a proximal portion of each of the at least two control wires being positioned through the slide assembly; and a control knob rotatably coupled to the housing for linearly translating the slide assembly, thereby enabling the slide assembly to separately manipulate each of said at least two control wires to effect a change in a deflection of said catheter.

Abstract: A catheter insertion device with a housing and an interior space. An access needle and a guide wire supported by and moveable relative to the access needle. A restraining element attached to a handle to limit the motion of the guide wire relative to the access needle. A catheter insertion device with a housing and an interior space. An access needle and a guide wire channel attached to the access needle. A guide wire supported by the guide wire channel. A handle attached to the guide wire to move the guide wire relative to the guide wire support channel. A method of introducing a catheter into a vessel by inserting a guide wire substantially contained within a housing into a vessel. Next, advance a catheter over the guide wire and into the vessel. Next, withdraw the guide wire out of the vessel and completely into the housing.