- Role
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- Date of registration
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EUDAMED last updated this device on Jun 1, 2026
B-06933289810227Finecare is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Guangzhou Wondfo Biotech Co., Ltd.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06933289810227B-06933289810227W201P0008(01)06933289810227
European Medical Device Nomenclature — the EU product classification assigned to this device.
W01021109C-REACTIVE PROTEINNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | May 17, 2023 | Dec 31, 2028 |
CN-MF-000000689No 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.