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- Date of registration
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EUDAMED last updated this device on May 22, 2026
697391169RZ01RH388994 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Finess Healthcare Group Co.,Ltd. Placed on the EU market in Norway. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
16978486830163697391169RZ01RH388994(01)16978486830163
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.
V010301BLADES WITH SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Norway; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NorwayPrimary placement | Still on market |
CN-MF-000004124No 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.