MatriDerm Flex Dermal Matrix
by Medskin Solutions Dr. Suwelack AG
Ref 83471-200Model MatriDerm
Active
CE MDR CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number11830GB450260817 | Date17 Aug 2026 | StatusWithdrawn |
| European Union | CE/MDD | Number42505690104T 04250569301490 | Date16 Jun 2026 | StatusActive |
Certificates
- 11830GB450260817 Cancelled
Technical documentation EU MDR
- Certifier
- DNV MEDCERT GmbH 0482
- Issued
- 17 Aug 2026
- Expires
- 21 Jan 2031
- Reason
- Other
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Trade Name
- MatriDerm Flex Dermal MatrixMatriDerm
- Model / Reference
- 83471-200, MatriDerm
- Primary DI / UDI-DI
- 04250569301490
- Basic UDI-DI
- 42505690104T, B-04250569301490
- EMDN Code
- P900404 Autologous graft supports
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000007747
Other devices from MedSkin Solutions Dr. Suwelack AG
Properties
Other properties (10)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No