Abstract: Provided herein is a disinfecting device, including a housing having a proximal end, a distal end having an opening therein, and a sidewall therebetween defining an interior in fluid communication with the opening, one or more flanges arranged at the distal end of the housing, and a disinfecting solution received within the interior, wherein the sidewall includes a deformable portion adjacent the distal end.

Abstract: Provided herein is a sepsis monitoring device including: a patch having a first side and an opposing second side, where the second side is adapted to adhere to human skin; a plurality of microneedles arranged on the second side of the patch and configured to penetrate the human skin to a depth sufficient to collect interstitial fluid when the patch is adhered to the human skin, where the plurality of microneedles are configured to collect the interstitial fluid when the patch is adhered to the human skin; and a sensor in fluid communication with the plurality of microneedles and configured to detect a biomarker indicating a sepsis condition or an onset of the sepsis condition when contacted with the interstitial fluid collected by the plurality of microneedles.

Abstract: Fluid applicators with precise volume dispensing control for dispensing fluids such as a disinfectant in a controlled manner. Such fluid applicators may include a barrel including a sidewall having an inside surface defining a chamber for retaining a fluid, an end press, a push rod disposed within the chamber, the push rod having a push button and a piercing tip, a cap attached to a port via a hinge to cover a hydrophobic filter disposed on the sidewall of the chamber, a one-way valve disposed on the outlet on a distal end of the barrel, a disinfectant disposed within the chamber; a housing having a base and an open proximal end; and a fluid applicator sponge disposed in the base of the housing. An alternate fluid may include a deformable end press, a plurality of volume scale markings on an outer surface of the barrel, a push rod, a one-way valve and applicator sponge.

Abstract: A medical device includes a luer cap, a needle housed in the luer cap, a luer tube in fluid communication with the needle, an actuator coupled at least one of the needle and the tube, a spring operatively associated with the actuator, and a vacuum tube for blood sample collection.

Abstract: A cap configured to engage at least a first connector and a second connector of different types includes a housing having a first end, an open second end, a sidewall extending between the first end and the second end, and a plurality of interfering protrusions extending inwardly from an inner surface of the sidewall configured to provide an interference engagement with the first connector or the second connector. The cap also includes an absorbent support positioned in the housing configured to contact portions of the first connector or the second connector, when the first connector or the second connecter is inserted into the housing and a seal mounted to a portion of the absorbent support configured to cover an opening of the first connector or the second connector when the first connector or the second connector is inserted into the housing.

Abstract: A catheter system may include a catheter assembly, which may include a catheter adapter and a catheter. The catheter system may include a needle assembly, a barrel, an introducer needle comprising a sharp distal tip, a needle hub coupled to the introducer needle and movably disposed within the barrel, and a spring disposed within the barrel. The catheter system may include a push button disposed in a locked position such that depression of the push button is inhibited. The push button may be configured to slide laterally or distally from the locked position to an unlocked position. When the push button is in the unlocked position and the barrel is spaced apart from the catheter adapter, the push button may be configured to depress. In response to depression of the push button, the spring may be configured to expand proximally and move the needle hub proximally within the barrel.

Abstract: Fluid applicators with precise volume dispensing control for dispensing fluids such as a disinfectant in a controlled manner are described herein. Such fluid applicators may include a barrel including a sidewall having an inside surface defining a chamber for retaining a fluid, an end press, a push rod disposed within the chamber, the push rod having a push button and a piercing tip, a cap attached to a port via a hinge to cover a hydrophobic filter disposed on the sidewall of the chamber, a one-way valve disposed on the outlet on a distal end of the barrel, a disinfectant disposed within the chamber; a housing having a base and an open proximal end; and a fluid applicator sponge disposed in the base of the housing. An alternate fluid may include a deformable end press, a plurality of volume scale markings on an outer surface of the barrel, a push rod, a one-way valve and applicator sponge.

Abstract: A disinfection cap for a male medical connector comprising a housing, a scrubbing foam having a plurality of slits disposed within a first cavity of the housing, a central post extending from the closed bottom of the housing and positioned within the first cavity of the housing, a foam jacket disposed on the central post and having a plurality of slits; and a central plug disposed in the center of the central post extending from the top wall of the central post and extending into the second cavity of the foam jacket. The inner surface of the foam jacket defines a second cavity.

Abstract: A cap configured to engage different types of connectors includes a housing, an absorbent support, and a seal. The housing includes a sidewall extending between a first end and a second end of the housing. The absorbent support is positioned in the housing. The seal is mounted to a portion of the absorbent support and is configured to cover an opening of a first connector or a second connector when one of the first connector or the second connector is inserted into the housing. The cap is configured to be secured to the first connector by an engagement between a portion of an inner surface of the sidewall of the housing and the first connector and to the second connector by an interference engagement between another portion of the inner surface of the sidewall of the housing and an outer surface of the second connector.

Abstract: A catheter system may include a catheter assembly and a needle assembly. The needle assembly may include a cover disposed over a push button. An inner surface of the cover may include a projection, and the cover may be configured to slide proximally. In response to the cover sliding proximally, the projection may be configured to contact the push button, and the push button may be configured to depress. The push button may include a living hinge. The housing may include a flange contacting a proximal end of the push button to prevent the proximal end of the button from being depressed. In response to bending of the living hinge, the push button may be configured to move distal to the flange and depress. In response to depression of the push button, the needle hub may move proximally within the barrel to retract the introducer needle.