An integrated intravenous catheter includes a catheter adapter having a catheter and an inlet, with the catheter configured to be inserted into a patient's vasculature, a needle-free connector comprising a first port, a second port positioned opposite the first port, and a side port positioned the first port and the second port, with the second port including a valve member, intermediate tubing extending between the inlet of the catheter adapter and the first port of the needle-free connector, and extension tubing extending from the side port of the needle-free connector.

A hybrid microneedle array and a method of fabricating the array is used for delivery of drugs, vaccines, and other therapeutic agents into tissues, including skin, heart, inner ear, and other tissues. The microneedle array can facilitate precise and reproducible intradermal delivery. Each microneedle has a dissolvable tip with a hollow body permitting the delivery of a variety of therapeutic agents into the skin. A fabrication process utilizes a two part mold to separately mold a dissolvable tip and a solid body portion of each microneedle in the array.

Disclosed is a system for real-time detection and annunciation of blood associated with menstruation and surgical wounds. The system comprises a real-time, wide area blood detector, communication means for relay of blood detection information, and annunciation means to inform the user of the emanation of blood. Various system embodiments include local and remote as well as covert and non-covert annunciation to users or medical personnel, various forms of real-time blood detection sensors, blood analysis capability, and smart bandage telemetry.

The invention generally relates to intracavitary medical devices and methods for using the devices. In one aspect, the devices comprise: a tube comprising a longitudinal body having opposed proximal and distal ends, and at least three lumens extending there between; and an expandable balloon region located at the distal end of the tube; wherein at least one lumen comprises at least one of: a drainage lumen which opens at a portion of the distal end of the tube and configured to allow fluid communication from a body cavity into the drainage lumen, an inflation lumen connected to an interior of the balloon region and configured to enable passage of a distending fluid to control expansion and contraction of the balloon region, and an instillation lumen which opens at a portion of the distal end of the tube and configured to allow a fluid to be introduced from the instillation lumen into the body cavity.

Methods and devices for collection of fluids, including cells and cellular materials, from the uterus. A device having a central tubing member to which, at least, a flexible tubing member and an absorbable member are connected at least at one point. The absorbable member is connected to at least one portion of the central tubing member and to at least one portion of the flexible tubing member. The devices are useful in methods of collection of uterine fluids, including blood, cells and cellular material.

The invention generally relates to enclosed desorption electrospray ionization probes, systems, and methods. In certain embodiments, the invention provides a source of DESI-active spray, in which a distal portion of the source is enclosed within a transfer member such that the DESI-active spray is produced within the transfer member.

In one embodiment of the disclosure, a method of monitoring a fetus in utero is disclosed that includes implanting a medical device into a patient's uterus, collecting fetal data using the medical device, and transmitting, e.g., wirelessly, the fetal data from the medical device to a receiver. In another embodiment, a medical monitoring system is disclosed that includes a first device that is implantable into a patient's uterus for collecting fetal data, and a second device that is configured and dimensioned for connection with the first device such that the fetal data is wirelessly communicable from the first device to the second device.

The present invention provides a coronary sinus inspiration catheter comprising a catheter head section and an extension tube, which are hollow tubular structures, the catheter head section and a distal section of the extension tube are substantially arc-shaped, the catheter head section comprises an arc section and a bend section, and its length is about 4-10 cm, the distal end is small (3-6 F) and the tube diameter of the catheter head section increase gradually toward the proximal end (6-12 F), the catheter head section is bent at a 15-45° angle at the position which has a distance of 0.5-1.5 cm from the distal end, the bend section is a straight or slightly arc-shaped structure. The catheter head section is provided with an end hole and a plurality of side holes, and is equidistantly provided with radiopaque markers from the distal end to the proximal end.

A kit and a method are disclosed for collecting and preparing a biological sample for testing where the sample is to be mixed with a buffer prior to being tested.

The invention generally relates to enclosed desorption electrospray ionization probes, systems, and methods. In certain embodiments, the invention provides a source of DESI-active spray, in which a distal portion of the source is enclosed within a transfer member such that the DESI-active spray is produced within the transfer member.