- Role
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- Date of registration
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EUDAMED last updated this device on Dec 16, 2025
803348865Y06120902CTPY-TKCO CLV.M is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by F.G.P. s.r.l.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08052990115068803348865Y06120902CTPY-TKCO CLV.M(01)08052990115068
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.
Y061209KNEE ORTHOSESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 1 country total.
Placed on the market in Italy; per-country availability dates not published.
IT-MF-000043862No 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.