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EUDAMED last updated this device on May 25, 2026
B-08021118000159IT-MF-0000289011 warning recorded — scroll inside the panel to see all entries.
CW010Primary placement in Italy; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Dec 31, 2028 | |
| Austria | Dec 31, 2028 | |
| Belgium | Dec 31, 2028 | |
| Bulgaria | Dec 31, 2028 | |
| Cyprus | Dec 31, 2028 | |
| Czechia | Dec 31, 2028 | |
| Germany | Dec 31, 2028 | |
| Denmark | Dec 31, 2028 | |
| Estonia | Dec 31, 2028 | |
| EL | Dec 31, 2028 | |
| Spain | Dec 31, 2028 | |
| Finland | Dec 31, 2028 | |
| France | Dec 31, 2028 | |
| Croatia | Dec 31, 2028 | |
| Hungary | Dec 31, 2028 | |
| Ireland | Dec 31, 2028 | |
| Iceland | Dec 31, 2028 | |
| Liechtenstein | Dec 31, 2028 | |
| Lithuania | Dec 31, 2028 | |
| Luxembourg | Dec 31, 2028 | |
| Latvia | Dec 31, 2028 | |
| Malta | Dec 31, 2028 | |
| Netherlands | Dec 31, 2028 | |
| Norway | Dec 31, 2028 | |
| Poland | Dec 31, 2028 | |
| Portugal | Dec 31, 2028 | |
| Romania | Dec 31, 2028 | |
| Sweden | Dec 31, 2028 | |
| Slovenia | Dec 31, 2028 | |
| Slovakia | Dec 31, 2028 | |
| Türkiye | Dec 31, 2028 | |
| XI | Dec 31, 2028 |
(01)08021118000159
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q0299OPHTHALMIC DEVICES - OTHERNo 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.