Conveen
Ref 21380
Conveen (21380) is a Class I device made by Coloplast A/S, registered in EUDAMED on 14 Sep 2026 (Basic UDI-DI 570893229790193), active as of 25 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number570893229790193 | Date14 Sep 2026 | StatusActive |
Official records
- EUDAMED public site 570893229790193
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Conveen leg bag strap hooks and loops closure siliconized
- Model / reference
- 21380
- Primary DI / UDI-DI
- 05701780796026, 05701780770330, 05708932555364, 05701780787963
- Basic UDI-DI
- 570893229790193
- Unit of use DI
- 05701780796668, 05701780459297, 05708932555357, 05701780788168
- EMDN code
- A0680 Drainage and fluid collection devices - accessories
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- BelgiumNetherlandsGermanyDenmark
Manufacturer details
- EUDAMED SRN
- DK-MF-000025526
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