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EUDAMED last updated this device on May 27, 2026
69368888CPSB013RELEPHANT IV is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Zhejiang YiGao Medical Technology Co., Ltd.. Placed on the EU market in Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0693744045100769368888CPSB013RCPS14040B-EU(01)06937440451007
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.
U090399SINGLE-USE INSTRUMENTS FOR UROGENITAL ENDOSCOPY - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Ireland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| IrelandPrimary placement | Still on market |
CN-MF-000032913No 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.