Alterna
Ref 13955
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number57089322975508U | Date12 Dec 2025 | StatusActive |
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- Withdrawn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
- Trade Name
- AlternaAssura
- Device Name
- Assura/Alterna (New Generation) ostomy bag 2-piece open
- Model / Reference
- 13955
- Primary DI / UDI-DI
- 05701780809863, 05701780818827, 05701780760805, 05708932345088, 05701780772136, 05708932152693, 05701780771528
- Basic UDI-DI
- 57089322975508U
- Unit of Use DI
- 05701780097505, 05701780097482, 05701780097611, 05701780097475, 05701780097635, 05701780097673, 05701780097574
- EMDN Code
- A10020202, A10020302
- Device Class
- Class I
- EU market of registration
- ItalyIrelandLiechtensteinEstoniaDenmarkPortugalNorway
Manufacturer details
- EUDAMED SRN
- DK-MF-000025526
Other devices from Coloplast A/S
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No