FinnComfort
by Waldi Schuhfabrik GmbH 1,000+ variants
Ref 02780-902680
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 | Number4030457-FinnCo-001-MN | Date8 May 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- Withdrawn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
- Model / Reference
- 02780-902680
- Primary DI / UDI-DI
- 00691812907894, 00691812907931, 00691812907849, 00691812907924, 00691812907917, 00691812907887, 00691812907870, 00691812907832, 00691812907856, 00691812907863, 00691812907900
- Basic UDI-DI
- 4030457-FinnCo-001-MN
- Direct Marketing DI
- 0069181290789400691812907931006918129078490069181290792400691812907917006918129078870069181290787000691812907832006918129078560069181290786300691812907900
- EMDN Code
- Y063303 Ready-made orthotic shoes
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000016907
Other devices from Waldi Schuhfabrik GmbH
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Reusable: 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