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EUDAMED last updated this device on Jun 6, 2024
805274210Auvita3GYaluSTYLE® + S is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by S.A.L.F. S.p.A. Laboratorio Farmacologico. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08052742102049805274210Auvita3GSISSV025010(01)08052742102049
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.
P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES6 warnings recorded — scroll inside the panel to see all entries.
CW001CW009CW007CW010CW011CW032Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market |
IT-MF-000010720Certificate health across this manufacturer's portfolio.
CVD005526IssuedCVD005426IssuedCVD0016230123IssuedCSQ0004231223SupplementedCVD000823IssuedCVD0002230623SupplementedCSQ0004231223CVD0002230623805274210LazuLy22On the marketAC 113 mmol/L 2:1 (Citrate Anticoagulant Solution 113 mmol/L 2:1)805274210CRRTScE4On the marketAC 113 mmol/L 2:1 (Citrate Anticoagulant Solution 113 mmol/L 2:1)805274210CRRTScE4On the marketActiCoal805274210AcCoalJYOn the marketActiCoal805274210AcCoalJYOn the market