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EUDAMED last updated this device on May 20, 2026
805957100PROTESICL.2MSKAC 5542 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by ZIACOM ITS S.r.l.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08059571003721805957100PROTESICL.2MSKAC 5542(01)08059571003721
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.
P01020180DENTAL IMPLANTS - ACCESSORIESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 7 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Estonia | Still on market | |
| Spain | Still on market | |
| Croatia | Still on market | |
| Romania | Still on market |
IT-MF-000028897Certificate health across this manufacturer's portfolio.
0425-MDR-030185-00Issued