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EUDAMED last updated this device on Jun 7, 2022
376036546NEOD-STD-NIPDNEO HYDRA is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by ACIME FRAME. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03760365460297376036546NEOD-STD-NIPDNEOD029(01)03760365460297
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V080603TREATMENT, DIAGNOSIS AND MONITORING MEDICAL BEDSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 1 country total.
Placed on the market in France; per-country availability dates not published.
FR-MF-000016067No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.