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EUDAMED last updated this device on May 28, 2026
4050824MPKOYEMP.KO1-200.100.10 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Wulff Med Tec GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
040508241462824050824MPKOYEMP.KO1-200.100.10(01)04050824146282
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.
V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market |
DE-MF-000010006No 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.