- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 29, 2026
57089322975719418401 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Coloplast A/S. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0570178025084957089322975719418401(01)05701780250849
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.
A100199DEVICES FOR ABDOMINAL OSTOMY - ONE PIECE - OTHER1 warning recorded — scroll inside the panel to see all entries.
CW025No certificate specifically references this device's Basic UDI-DI.
Primary placement in Belgium; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Still on market | |
| Luxembourg | Still on market |
DK-MF-000025526No 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.