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EUDAMED last updated this device on Mar 24, 2026
805744052C0204MIT-MF-000040696No 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.1 warning recorded — scroll inside the panel to see all entries.
CW999Primary placement in Italy; available across 19 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jan 1, 2022 | Still on market |
| Austria | Jan 1, 2022 | Still on market |
| Belgium | Jan 1, 2022 | Still on market |
| Germany | Jan 1, 2022 | Still on market |
| Denmark | Jan 1, 2022 | Still on market |
| Estonia | Jan 1, 2022 | Still on market |
| EL | Jan 1, 2022 | Still on market |
| Spain | Jan 1, 2022 | Still on market |
| Finland | Jan 1, 2022 | Still on market |
| France | Jan 1, 2022 | Still on market |
| Ireland | Jan 1, 2022 | Still on market |
| Lithuania | Jan 1, 2022 | Still on market |
| Luxembourg | Jan 1, 2022 | Still on market |
| Latvia | Jan 1, 2022 | Still on market |
| Netherlands | Jan 1, 2022 | Still on market |
| Norway | Jan 1, 2022 | Still on market |
| Poland | Jan 1, 2022 | Still on market |
| Portugal | Jan 1, 2022 | Still on market |
| Sweden | Jan 1, 2022 | Still on market |
(01)80574405200656
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.
Y063099NON-EXTREMITY PROSTHESES - OTHER