A securement assembly for supporting and stabilizing a vascular access device, such as a tunneled central venous access devices (CVAD) or a surgical drain, is provided herein. The securement assembly may comprise a base and a lid. The base may include a central post about/around which the external portion of the access device or surgical drain may be wrapped. The lid may extend from the base and may be configured to cover the external portion of the access device or surgical drain (when installed). In various embodiments, the base and the lid collectively define an annular chamber around the central post of the base.

An apparatus to couple a drainage reservoir to a patient is disclosed. The apparatus comprises a device having, a first end, a second end, and a tab with an orifice. The first end comprises an adhesive surface. Further, the apparatus includes a clip attached to the orifice in the tab of the device. The first end of the device is attached to the body of the patient, and the clip is coupled to the strap on the drainage reservoir such that the drainage reservoir is coupled to the body of the patient with the help of the device and the included clip.

A low profile catheter system includes a catheter hub with proximal, distal, and intermediate portions, a stabilization surface located on an underside, and a receptacle located within a top surface. A substantially linear flow path extends from an opening at the distal portion to an inlet located within the intermediate portion and allows fluid to flow between the distal and intermediate portions. The inlet of the flow path is located between the proximal and distal portions. A base connector has a fluid path extending through at least a portion of the base connector and between a first opening located nearer a first end and a second opening. The fluid path is fluidly connected to the inlet of the flow path and a second end of the base connector is retained within the receptacle by the proximal portion when the base connector is received by the receptacle.

In one embodiment, the dressing has a base which is to be adhered to a patient about a catheter site, an aperture in the base to pull a catheter line through and a cover with a window that is folded over and onto the base in a sealed manner. In another embodiment, the dressing has two covers with windows for folding over separate sections of a base to seal in the components of a catheter assembly with multiple catheters extending from a common housing.

An applicator of one aspect for applying a sheet member to skin includes a body having a bottom surface facing the skin and a first guide configured to guide the sheet member to a space between the skin and the bottom surface, in which the sheet member is applied to the skin after being folded in the space.

A method of stabilizing a tube at a stoma of a patient includes providing a stabilizing device having a base portion and a tube holding portion that is attached at the base portion via at least two legs and that, with the base portion affixed to the patient, is spaced from the stoma of the patient. The tube holding portion has a passageway therethrough that is configured to receive the tube that passes through the stoma. The tube holding portion may be adjusted to position the tube in a free-flow orientation or a restricted-flow orientation. The tube holding portion may include a disinfecting wiping element. The stabilizing device may have pads coupled to respective legs via an elastomeric connecting element to allow for adjustment of the pads relative to the legs. The tube holding portion may include flexible tabs that deflect to enlarge an effective diameter of the passageway.

A holder for securing a venous access device to a patient may include a flexible substrate having an upper surface, a lower surface, and an outer perimetal surface. An adhesive layer may overlay the lower surface of the flexible substrate. The adhesive layer may have an adhesive for adhering to skin of the patient. The holder may further include a hydrophilic matrix integrated into at least a portion of the adhesive layer, at least one solvent reservoir disposed on the upper surface of the flexible substrate, and a connector secured to the outer perimetal surface. The connector may have a first end for connection to a needle assembly and a second end for connection to an IV fluid line.

A facial skin indentation preventer has a central base core surrounded by an entrapment flap and a securing flap. The core and flaps have at least a single layer of soft moleskin, felt, or similar material forming an outer skin-contact layer that is non-adhesive. A rigid component is attached to the outer skin-contact layer in a center of the preventer, thereby defining a central base core. The central base core can have a cannula or similar item placed thereon. The flaps are then folded inwards, over the rigid component, creating a cannula pocket above the rigid component and entrapping and holding the cannula therein. An entrapment hinge and securing hinge ensure the folds remain rounded and soft. A flap attachment is used to lock the securing flap to the entrapment flap and ensure the cannula stays within the cannula pocket.

An apparatus includes a pad assembly, an injector assembly, an injector driver, and a fluid source. The pad assembly is sized and configured to be placed on a forehead of a patient. The injector assembly includes a body, a flexible cannula, and a needle. The body is configured to be removably secured to the pad assembly. The cannula is sized to be inserted through an incision in an eye of a patient. The needle is slidably disposed in the cannula. The injector driver is operable to drive the needle longitudinally relative to the flexible cannula. The fluid source assembly is in fluid communication with the needle.

Systems, methods and devices are described including a medical device subassembly including a magnetic feature. Systems include such a catheter adapter subassembly or needle subassembly or guidewire introducer subassembly and a wire including a magnetic feature, and relative movement of the catheter adapter subassembly or needle subassembly or guidewire introducer subassembly and the wire can be determined using an magnetometer.