- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 15, 2026
69509009CEAGWMN0695090092198869509009CEAGWMNGW352JF(01)06950900921988
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.
C04020102PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILICNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Slovakia; available across 15 countries total.
| Country | On market since | Until |
|---|---|---|
| SlovakiaPrimary 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 | |
| EL | 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-000009966No 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.