Easiflex
Ref 14681
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 | Number57089322975579A | Date24 Aug 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- Withdrawn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
- Device Name
- Easiflex ostomy bag 2-piece open
- Model / Reference
- 14681
- Primary DI / UDI-DI
- 05708932170970, 05708932164399, 05708932201346, 05708932169264, 05708932220330, 05708932224246, 05708932069328, 05708932400114
- Basic UDI-DI
- 57089322975579A
- Unit of Use DI
- 05708932960250, 05701780122290, 05701780122207, 05701780122160, 05701780122177, 05701780122313, 05701780122320, 05701780122221
- EMDN Code
- A10020202, A10020302
- Device Class
- Class I
- EU market of registration
- GermanyDenmarkFinlandNetherlandsBelgiumLiechtensteinSlovakiaItaly
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