Ceracell®
Ref 9001 102 001Model CERACELL®
Active
CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-+ECUR90011020011 +ECUR90011020011 | Date23 May 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
EU market availability
Made available in 12 countries, as listed in EUDAMED:
- Austria since 5 Oct 2010
- Belgium since 5 Oct 2010
- Bulgaria since 5 Oct 2010
- Denmark since 5 Oct 2010
- Finland since 5 Oct 2010
- Germany since 5 Oct 2010
- Iceland since 5 Oct 2010
- Luxembourg since 5 Oct 2010
- Netherlands since 5 Oct 2010
- Norway since 5 Oct 2010
- Slovenia since 5 Oct 2010
- Sweden since 5 Oct 2010
Specification
- Model / Reference
- CERACELL®, 9001 102 001
- Primary DI / UDI-DI
- +ECUR90011020011
- Basic UDI-DI
- B-+ECUR90011020011
- EMDN Code
- P900402 Resorbable filling and reconstruction devices
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000008316
Other devices from Curasan AG
Properties
Other properties (9)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No