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EUDAMED last updated this device on Jun 3, 2026
8033439ASSUFILM-PDOUG02FVPMSAQ is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by ASSUT EUROPE SPA. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
180334393798808033439ASSUFILM-PDOUG02FVPMSAQ(01)18033439379880
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.
H010101010103POLYDIOXANONE MONOFILAMENT WITHOUT NEEDLEPrimary placement in Italy; available across 8 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Bulgaria | Still on market | |
| Cyprus | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Romania | Still on market |
IT-MF-000018178Certificate health across this manufacturer's portfolio.
CVD0032240124SupplementedCSQ0013230724SupplementedCVD003124IssuedCVD0030240124SupplementedCVD002023IssuedCVD001423IssuedCSQ0013230524CVD003124