Emed Technologies Corporation

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Web: http://emedicaldevices.com
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Address: 1264 Hawks Flight Court, Suite 200, El Dorado Hills, California 95762, USA
Phone: +1-(888)-550-6500 | Fax: +1-(888)-879-6991 | Map/Directions >>

Profile: Emed Technologies Corporation is a designer and manufacturer of medical devices. Our infusion(IV) pump is ideal for ambulatory and hospital use, and offers enhanced simplicity for various therapies including immune globulin administration, pain management, or chemotherapy & antibiotic therapies. Our Huber needles are used in conjunction with patient implanted ports, and are used for patient therapies requiring repeated vascular access. Our port systems are used for the withdrawal of blood samples and the infusion of medications, parenteral nutritional solutions, blood products & imaging solutions.

FDA Registration Number: 2523167

8 Products/Services (Click for related suppliers)

• Fluid Delivery Tubing (FDA Code: FPK / 880.5440)

An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.

• Infusion Line Filter (FDA Code: FPB / 880.5440)

• Infusion Therapy Kits

• Infusion Therapy Kits, Tubing & Bags

• Infusion Therapy Systems

• Intravenous Administration Kit (FDA Code: FPA / 880.5440)

• Non-Implantable Electrical Stimulator (FDA Code: KPI / 876.5320)

A nonimplanted electrical continence device is a device that consists of a pair of electrodes on a plug or a pessary that are connected by an electrical cable to a battery-powered pulse source. The plug or pessary is inserted into the rectum or into the vagina and used to stimulate the muscles of the pelvic floor to maintain urinary or fecal continence. When necessary, the plug or pessary may be removed by the user. This device excludes an AC-powered nonimplanted electrical continence device and the powered vaginal muscle stimulator for therapeutic use (884.5940).

• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570)

A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.