A medical dispensing device which includes a catheter, an applicator tip at a distal end of the catheter, the catheter and the applicator tip defining a lumen having a longitudinal axis and a distal opening, a plunger in the lumen and movable along the longitudinal axis, and a plurality of elements in the lumen proximal to the distal opening and distal to the plunger, the plurality of elements stacked along the longitudinal axis for dispersement of one element at a time through the distal opening via a force applied by the plunger.

A ventriculostomy patch system is disclosed herein. The ventriculostomy patch system including a base-ring, and a window assembly. The base-ring includes a circular body, with the circular-body having an outer-surface, an inner-surface, a top-surface, and a bottom-surface. The bottom-surface includes a catheter-notch; the catheter-notch is configured for removably retaining a ventriculostomy catheter. The base-ring further includes at least two dome-tabs, each of the at least two dome-tabs located upon the outer surface of the base-ring. Preferably, the base-ring is constructed from anti-microbial materials. The window assembly includes an external-ring and a window, where the window assembly is removably affixable to the top-surface of the base-ring.

An integrated vascular delivery system and method of use, the system including: a frame having a catheter hub that provides a first anchoring point on the patient and receives a catheter insertable in the patient to transfer fluid at an insertion site, a stabilization hub that provides a second anchoring point on the patient, at least one lateral member extending between the catheter and stabilization hubs, and a fluidic channel. The frame operates in a folded configuration in which the hubs are coupleable and an unfolded configuration in which the anchoring points are distributed around the insertion site to anchor the frame to the patient, thereby stabilizing the catheter. In some embodiments, the system further includes a septum that helps prevent fluid leakage from the catheter hub, or a needle shield that covers the distal end of a needle used during catheter insertion.

A substrate based skin contact material formed from a hydrocolloid having a silicone based component extending over regions of the substrate surface. The adhesive is formed non-continuously over the substrate to provide areas devoid of adhesive to allow appreciable moisture transfer between the skin and substrate and improve the skin friendliness of the material during use and allow convenient removal with avoidance of skin irritation.

A stabilisation system for securing a medical device such as a catheter to tissue, in particular skin, the stabilisation system comprising a main body having a first section and a second section displaceable relative to one another to translate the system between an undeployed state and a deployed state, each section including an array of microneedles extending from a tissue contacting surface of the body and which penetrate the skin in response to the above displacement, the stabilisation system further comprising a closure member displaceable between an open position exposing a retention zone on the body and a closed position at least partially occluding the retention zone, within which retention zone the catheter or other medical device may be captured.

A closed-circuit dressing system for preventing moisture contacting PICC sites is provided. The closed-circuit dressing system include a breathable bag for harboring the PICC line(s) and a dressing film that envelopes the PICC site, wherein a moisture indicator ring provided by the dressing film indicates moisture penetrating a dressing reinforcement along the periphery of the dressing film.

A securement device configured to secure an external portion of a medical device to the skin surface of a patient after an internal portion of the device has been placed in the patient is disclosed. The securement device includes a retainer that is employed to securely retain the external portion of the medical device in place. The retainer is attached to a base, such as an adhesive pad that adhesively attaches to the skin surface. In one embodiment, therefore, a retainer comprises a body defining a channel configured to receive therein a portion of the medical device, and at least one foot extending from the body that is configured to stabilize the retainer with respect to a skin surface. The retainer body further includes a nose that is configured to deflect a portion of the external portion of the medical device toward the skin insertion site.

A catheterization system for treatment of patients can include a peripherally inserted central catheter comprising a catheter tube joined to an extension leg with a junction and a securement device that fits around a portion of the junction to inhibit movement. The catheter tube can include a taper proximate the junction, the taper transitioning the catheter tube from a larger outer diameter and a larger wall thickness to a smaller outer diameter and a smaller wall thickness. The taper and thicker wall thickness near the junction can help prevent damage to the catheter tube near the junction when bent (e.g., to secure a proximal region of the catheter to a patient's arm). The securement device can configured to fit around an outer diameter of the junction to inhibit movement of the junction when the junction is held in the securement device.

An integrated catheter includes a catheter adapter having a catheter and an inlet, the catheter configured to be inserted into a patient's vasculature. The integrated catheter also includes a near-patient access port having a first port at a first end and a female luer connector at a second end, as well as intermediate tubing extending between the inlet of the catheter adapter and the first port of the near-patient access port. Additionally, the integrated catheter includes a stabilization platform configured to stabilize at least the near-patient access port on a patient's skin.

Subcutaneous access hub embodiments are discussed herein that include housing embodiments having a plurality of cannula ports and a fluid passageway network that allows fluid communication between a fluid source and the plurality of cannula access ports. Such a configuration may allow a user such as a patient or clinician to releasably secure the housing to an outside surface of the patient's skin. Multiple locations on the patient's skin may then be accessed for deployment of one or more delivery cannulas via a plurality of cannula ports for delivery of fluid and from the fluid source to multiple subcutaneous locations below the patient's skin and timely movement of cannula access in the patient's skin without the need for relocating the housing.