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EUDAMED last updated this device on Nov 26, 2021
B-08053677040079AIFLUME001 is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by CENTERVUE S.P.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08053677040079B-08053677040079AIFLUME001(01)08053677040079
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12120199OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jun 24, 2016 | May 25, 2024 |
| Austria | Jun 24, 2016 | May 25, 2024 |
| Belgium | Jun 24, 2016 | May 25, 2024 |
| Bulgaria | Jun 24, 2016 | May 25, 2024 |
| Cyprus | Jun 24, 2016 | May 25, 2024 |
| Czechia | Jun 24, 2016 | May 25, 2024 |
| Germany | Jun 24, 2016 | May 25, 2024 |
| Denmark | Jun 24, 2016 | May 25, 2024 |
| Estonia | Jun 24, 2016 | May 25, 2024 |
| EL | Jun 24, 2016 | May 25, 2024 |
| Spain | Jun 24, 2016 | May 25, 2024 |
| Finland | Jun 24, 2016 | May 25, 2024 |
| France | Jun 24, 2016 | May 25, 2024 |
| Croatia | Jun 24, 2016 | May 25, 2024 |
| Hungary | Jun 24, 2016 | May 25, 2024 |
| Ireland | Jun 24, 2016 | May 25, 2024 |
| Iceland | Jun 24, 2016 | May 25, 2024 |
| Liechtenstein | Jun 24, 2016 | May 25, 2024 |
| Lithuania | Jun 24, 2016 | May 25, 2024 |
| Luxembourg | Jun 24, 2016 | May 25, 2024 |
| Latvia | Jun 24, 2016 | May 25, 2024 |
| Malta | Jun 24, 2016 | May 25, 2024 |
| Netherlands | Jun 24, 2016 | May 25, 2024 |
| Norway | Jun 24, 2016 | May 25, 2024 |
| Poland | Jun 24, 2016 | May 25, 2024 |
| Portugal | Jun 24, 2016 | May 25, 2024 |
| Romania | Jun 24, 2016 | May 25, 2024 |
| Sweden | Jun 24, 2016 | May 25, 2024 |
| Slovenia | Jun 24, 2016 | May 25, 2024 |
| Slovakia | Jun 24, 2016 | May 25, 2024 |
| Türkiye | Jun 24, 2016 | May 25, 2024 |
| XI | Jun 24, 2016 | May 25, 2024 |
IT-MF-000017082No 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.G1 070221 0013