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Samarit Medical AG

CH-MF-000016280 · Switzerland · Zumikon

Samarit Medical AG is registered in the European database on medical devices as a manufacturer, with 21 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa21

Most frequent device types declared: Hightec, Rollbord Blue Transfer, Rollbord Transglide, Professional, Rollbord EcoLite.

Authorised representative in the Union: DE-AR-000014694.

United States market access

FDA establishment registerRegistered with FDA
Matched entrySAMARIT MEDICAL AG (CH) · FDA 3014872186
Devices in EUDAMED21
Country of registrationSwitzerland

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