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EUDAMED last updated this device on Jun 1, 2026
73955026115152BN571114 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Mediplast AB. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0739550209011073955026115152BN571114(01)07395502090110
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.
R030199RESPIRATORY MASKS - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Sweden; available across 19 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Denmark | Still on market | |
| Spain | Still on market | |
| Finland | Still on market | |
| France | Still on market | |
| Hungary | Still on market | |
| Ireland | Still on market | |
| Iceland | Still on market | |
| Italy | Still on market | |
| Luxembourg | Still on market | |
| Malta | Still on market | |
| Netherlands | Still on market | |
| Norway | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market |
SE-MF-000000885No 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.