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Eu Medical Device Regulations Equipment Supplied In Usa
2 equipment items found
by:Sterling Medical Devices based inMoonachie, NEW YORK (USA)
All medical devices sold in the EU must have a Clinical Evaluation Report (CER) as part of its technical documentation to satisfy the new EU Medical Device Regulation (MDR) requirements. A comprehensive analysis of pre- and post-market data relevant to a medical ...
Manufactured by:Vitalograph Inc based inLenexa, KANSAS (USA)
The Vitalograph 6MWT solution includes a tablet running the 6MWT protocol, SPO2 monitor and kit to mark the ...