- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 28, 2026
3700535100003PKCH-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 5 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Jan 1, 2005 | Still on market |
| Belgium | Aug 9, 2018 | Still on market |
| Ireland | Feb 28, 2018 | Still on market |
| Italy | Dec 3, 2019 | Still on market |
| Luxembourg | Aug 9, 2018 | Still on market |
(01)03700535143162
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.
L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER