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EUDAMED last updated this device on Jan 10, 2022
871992590200FEAOP-Film S279 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Eurotape B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08719925902529871992590200FEAS279.2021-2X5(01)08719925902529
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.
T02010101INCISION DRAPES, WITHOUT ANTIBACTERIAL AGENT2 warnings recorded — scroll inside the panel to see all entries.
CW009CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Netherlands; available across 9 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Mar 27, 2020 | Still on market |
| Austria | Mar 27, 2020 | Still on market |
| Czechia | Mar 27, 2020 | Still on market |
| Germany | Mar 27, 2020 | Still on market |
| Spain | Mar 27, 2020 | Still on market |
| Ireland | Mar 27, 2020 | Still on market |
| Italy | Mar 27, 2020 | Still on market |
| Poland | Mar 27, 2020 | Still on market |
| Portugal | Mar 27, 2020 | Still on market |
NL-MF-000001956No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.