Electro Medical Systems SA

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Web: http://www.ems-company.com
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Address: Ch. De La VuarpilliA"re 31, Nyon 1260, Switzerland
Phone: +41-(22)-99 44 700 | Fax: +41-(22)-99 44 701 | Map/Directions >>

Profile: Electro Medical Systems SA is involved in the development and production of medical devices. Our LithoClastr device is an intracorporeal shockwave lithotriptor that is useful for the treatment of kidney, ureteric and bladder stones. Our OrthoClastr system provides good clinical outcome for the removal of non-cemented prosthesis stems.

FDA Registration Number: 8030987
US Agent: Dinora Delgado / Electro Medical Systems Corporation
Phone: +1-(972)-690-8382 Fax: +1-(972)-690-8981 E-Mail:

10 Products/Services (Click for related suppliers)

• Cement Removal Extraction System (FDA Code: LZV / 888.4580)

A sonic surgical instrument is a hand-held device with various accessories or attachments, such as a cutting tip that vibrates at high frequencies, and is intended for medical purposes to cut bone or other materials, such as acrylic.

• Electrohydraulic Lithotriptor (FDA Code: FFK / 876.4480)

An electrohydraulic lithotriptor is an AC-powered device used to fragment urinary bladder stones. It consists of a high voltage source connected by a cable to a bipolar electrode that is introduced into the urinary bladder through a cystoscope. The electrode is held against the stone in a water-filled bladder and repeated electrical discharges between the two poles of the electrode cause electrohydraulic shock waves which disintegrate the stone.

• Fluid Evacuator System (FDA Code: FHF / 876.4370)

A gastroenterology-urology evacuator is a device used to remove debris and fluids during gastroenterological and urological procedures by drainage, aspiration, or irrigation. This generic type of device includes the fluid evacuator system, manually powered bladder evacuator, and the AC-powered vacuum pump.

• Gastro-Urology Evacuator (FDA Code: KQT / 876.4370)

• Infusion Pump Tester

• Knee Joint Femorotibial Metal/Polymer Non-constrained Cemented Prosthesis (FDA Code: HSX / 888.3520)

A knee joint femorotibial metal/polymer non-constrained cemented prosthesis is a device intended to be implanted to replace part of a knee joint. The device limits minimally (less than normal anatomic constraints) translation in one or more planes. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral condylar resurfacing component or components made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components made of ultra-high molecular weight polyethylene and are intended for use with bone cement (888.3027).

• Pneumatic Powered Orthopedic Surgical Instrument & Accessory (FDA Code: HSZ / 878.4820)

• Pneumatic-Powered Surgical Instrument Motor (FDA Code: GET / 878.4820)

• Shock-Wave Generator For Pain Relief (FDA Code: NBN)

• Sonic Surgical Instrument and Accessory (FDA Code: JDX / 888.4580)