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EUDAMED last updated this device on Feb 11, 2025
8027864SIFIMDF33NA1131CCZ is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by SIFI S.p.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
080278640734308027864SIFIMDF33NA1131CCZ(01)08027864073430
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.
P030102100302IOLs, APHAKIC, MULTIFOCAL, TORIC, HYDROPHILIC ACRYLIC7 warnings recorded — scroll inside the panel to see all entries.
CW999CW011CW010CW009CW001CW020CW007Primary placement in Italy; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Belgium | Still on market | |
| Germany | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Lithuania | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Romania | Still on market | |
| Türkiye | Still on market |
IT-MF-000020853Certificate health across this manufacturer's portfolio.
027-00-06-MDRSupplementedCSQ0020240225SupplementedCVD0015230125Issued028-00-02-MDRSupplemented028-00-02-MDR