Alterna
Ref 14273
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 | Number57089322976108M | Date12 Feb 2026 | 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- Withdrawn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 (Original) ostomy baseplate convex
- Model / Reference
- 14273
- Primary DI / UDI-DI
- 05701780935210, 05701780903783, 05701780890328, 05701780874625, 05701780934862
- Basic UDI-DI
- 57089322976108M
- Unit of Use DI
- 05701780108478, 05701780108553, 05701780108539, 05708932961158, 05701780108515
- EMDN Code
- A1002010402 Universal plates for abdominal stoma (colo-, ileo-, urostomy) with introflex stoma
- Device Class
- Class I
- EU market of registration
- ItalyBelgiumDenmarkGermanyIreland
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