- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 28, 2026
3700535100015PSCH-MF-000018319No 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.Primary placement in France; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Dec 3, 2025 | Still on market |
| Belgium | Dec 3, 2025 | Still on market |
| Luxembourg | Dec 3, 2025 | Still on market |
(01)03700535169360
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.
L091201ORTHOPAEDIC SURGERY RASPS, REUSABLE