Alterna
Ref 13986
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- Withdrawn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
- 13986
- Primary DI / UDI-DI
- 05708932167710, 05708932594141, 05701780718257, 05708932327510, 05701780809900, 05701780760898, 05701780818926, 05701780772211, 05701780760164, 05701780771610
- Basic UDI-DI
- 57089322975508U
- Unit of Use DI
- 05701780099943, 05708932594165, 05701780100199, 05701780100205, 05701780099981, 05701780100052, 05701780100229, 05701780100434, 05708932961868, 05701780100243
- EMDN Code
- A10020202, A10020302
- Device Class
- Class I
- EU market of registration
- CroatiaBulgariaNetherlandsLithuaniaItalyLiechtensteinIrelandDenmarkGermanyNorway
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