A system for treatment of an open wound in a chest of a patient is disclosed. The system includes a seal membrane configured to adhere to the chest and having an air passage. The system also includes a mechanism removably coupled to the seal membrane over the air passage. The mechanism is configured to allow air to pass through the mechanism in a first direction and not to pass in a second direction opposite the first direction.

A fluid connector, including a fluid path portion having an integral cannula extending in a first direction from a interior surface, and a latching portion secured to the fluid path portion and having a pair of displaceable arms. Each arm includes a connector latch disposed at a first cantilevered end of the arm, and an activation lever disposed at an opposite cantilevered end of the arm and extending in a second direction, not parallel to the first direction. A portion of the activation lever includes a first lateral tactile feature aligned substantially parallel to the first direction to prevent forward slippage of the fluid connector from a user's grasp in the second direction, and a portion of the activation lever includes a lateral tactile feature aligned substantially parallel to the second direction to prevent slippage of the fluid connector from a user's grasp in the first direction.

A vascular access device with arteriovenous fistula support includes a top portion and a bottom portion. The top portion has a partial artery channel, a partial vessel channel, and a partial arteriovenous joint between the partial artery channel and the partial vessel channel, where the partial vessel channel has a vascular access aperture for exposing the vessel. The bottom portion has a corresponding partial artery channel, partial vessel channel, and partial arteriovenous joint between the partial artery channel and the partial vessel channel. When the top portion is coupled to the bottom portion, the two partial artery channels couple together to form an artery channel, the two partial vessel channels couple together to form a vessel channel, and the two partial arteriovenous joints couple together to form an arteriovenous joint for an arteriovenous fistula.

Disclosed are toggling vascular access port and methods of deploying thereof. The port includes a port body coupled with a septum member covering a cavity defined by the port body, and at least one port body extension restrictedly movable along an at least one defined route on the port body. The port is selectively changeable from a delivery configuration to a deployed configuration by moving the at least one port body extension along the at least one defined route wherein the at least one port body extension and the port body are approximated along a median plane of the port body and laterally opposing portions of the at least one port body extension are parted transversely to the median plane, thereby reducing length-to-width ratio of the toggling vascular access port.

A releasable coupling mechanism for coupling a delivery catheter and a dilator. The delivery catheter comprising a delivery catheter hub at the proximal end and the dilator comprising a dilator hub at the proximal end. The proximal end of the delivery catheter hub comprises a coupling member for releasably receiving a raised portion which is positioned at a distal end of the dilator hub. The coupling member has a pair of engagement members positioned on opposing sides of the coupling member and configured to releasably engage the raised portion. The delivery catheter hub further comprising at least one indicia on the housing. The indicia indicate an orientation of the delivery catheter hub such that the dilator hub disengages from the coupling member by simultaneously deflecting the pair of engagement members.

This invention concerns improved single use caps or covers for vascular access devices such as needlefree connectors that are used, for example, in intravenous administration sets and extension sets. Removal of a single use cap or cover according to the invention from a vascular access device destroys the cap such that it cannot be reused. Such single use caps and covers will help ensure compliance with infection prevention protocols in healthcare settings, which will assist in reducing the incidence of healthcare-associated infections (HAIs), particularly catheter-related blood stream infections. Assemblies and kits its including such caps and covers, for example, IV administration and extension sets that include one or more needlefree connectors, as well as methods for using such caps and covers, are also described.

Medical devices and methods for making and using medical devices are disclosed. An example medical device may include an access valve that may be retrieved after implantation. The access valve may include a frame having a lumen, a self-expandable member extending through the lumen, and an elastic membrane extending through the lumen and a second end of the frame to releasably seal the lumen. The access valve may releasably attach to a wall of a patient and releasably seal an opening through the wall. The access valve may be attached to the wall by placing the frame adjacent the wall, extending the self-expandable member through the opening in the wall, and expanding the self-expandable member such that the self-expandable member applies a first force against the wall and a second force opposite the first force against the frame to sandwich the wall between the self-expandable member and the frame.

A venous access port assembly having a base, a peripheral surface, and a septum. The base defines an interior reservoir. The peripheral surface includes integrally molded X-ray discernable indicia identifying that the assembly is rated for power injection. The X-ray discernable indicia may extend through a height of the peripheral surface from a top surface to a bottom surface thereof. According to one aspect, the peripheral surface may be formed from X-ray discernable material, and the X-ray discernable indicia may be formed from the X-ray discernable material, or they may be formed by voids in the X-ray discernable material. According to another aspect, the peripheral surface may be formed from a radiotransparent or radiolucent material and applied with a radiopaque agent, and the X-ray discernable indicia may be one or more voids in the radiopaque agent or may be portions of the peripheral surface applied with the radiopaque agent.

A snap-fit cover is configured to snap fit to a dilator hub. The snap-fit cover is also configured to snap fit to the sheath-hub cap of the sheath hub.

A venous access port assembly having a base, a peripheral surface, and a septum. The base defines an interior reservoir. The peripheral surface includes integrally molded X-ray discernable indicia identifying that the assembly is rated for power injection. The X-ray discernable indicia may extend through a height of the peripheral surface from a top surface to a bottom surface thereof. According to one aspect, the peripheral surface may be formed from X-ray discernable material, and the X-ray discernable indicia may be formed from the X-ray discernable material, or they may be formed by voids in the X-ray discernable material. According to another aspect, the peripheral surface may be formed from a radiotransparent or radiolucent material and applied with a radiopaque agent, and the X-ray discernable indicia may be one or more voids in the radiopaque agent or may be portions of the peripheral surface applied with the radiopaque agent.