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EUDAMED last updated this device on Jun 3, 2026
8033439ASSUFILM-PDOUGFX825KMAQ 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.
380334394013638033439ASSUFILM-PDOUGFX825KMAQ(01)38033439401363
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.
H010101010102MOUNTED POLYDIOXANONE MONOFILAMENT WITH NEEDLE FOR VIDEO SURGERYPrimary 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.
CSQ0013230524SupplementedCVD003124IssuedCVD0030240124SupplementedCVD002023IssuedCVD001423IssuedCSQ0013230524CVD003124