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EUDAMED last updated this device on May 27, 2026
40495001820KM900938 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by PAUL HARTMANN AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0404950027207040495001820KM900938(01)04049500272070
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.
M040499DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHER3 warnings recorded — scroll inside the panel to see all entries.
CW011CW001CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 15 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market | |
| Cyprus | Still on market | |
| Denmark | Still on market | |
| Estonia | Still on market | |
| Spain | Still on market | |
| Finland | Still on market | |
| France | Still on market | |
| Croatia | Still on market | |
| Malta | Still on market | |
| Norway | Still on market | |
| Portugal | Still on market | |
| Sweden | Still on market | |
| Slovenia | Still on market | |
| Slovakia | Still on market | |
| Türkiye | Still on market |
DE-MF-000005861No 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.