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EUDAMED last updated this device on May 16, 2026
69509009CEGWSGHGSS354AF is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Shanghai INT Medical Instruments Co., Ltd.. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0695090095311869509009CEGWSGHGSS354AF(01)06950900953118
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.
C04020101PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, HYDROPHILICNo certificate specifically references this device's Basic UDI-DI.
Primary placement in EL; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| ELPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Still on market | |
| Cyprus | Still on market | |
| Germany | Still on market | |
| Denmark | Still on market | |
| Estonia | Still on market | |
| Finland | Still on market | |
| Croatia | Still on market | |
| Ireland | Still on market | |
| Latvia | Still on market | |
| Malta | Still on market | |
| Netherlands | Still on market | |
| Poland | Still on market |
CN-MF-000009966Certificate health across this manufacturer's portfolio.
3QMS-MDR-0068/06/2025Issued1QMS-MDR-0068/06/2025Issued