Brava
Ref 12072
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 | Number57089322976889S | Date23 Jul 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- Withdrawn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
- Brava Elastic Tape
- Model / Reference
- 12072
- Primary DI / UDI-DI
- 05708932577199, 05708932614597, 05708932577250, 05708932786942, 05708932577076, 05708932757706, 05708932602297, 05701780319416, 05708932577137, 05708932597531, 05701780268028, 05708932597593, 05708932578455, 05708932609227, 05708932607346
- Basic UDI-DI
- 57089322976889S
- EMDN Code
- A108001 Rings / bezels / plates for peristomal skin
- Device Class
- Class I
- EU market of registration
- ItalyNorwayIrelandPortugalGermanyGreeceNetherlandsSlovakiaLiechtensteinBelgiumCyprusAustriaDenmarkCzechiaSpain
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