FinnComfort
by Waldi Schuhfabrik GmbH 1,000+ variants
Ref 02783-902502
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- Withdrawn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
- 02783-902502
- Primary DI / UDI-DI
- 00691812663394, 00691812663479, 00691812663400, 00691812663424, 00691812663417, 00691812663455, 00691812663431, 00691812663370, 00691812663462, 00691812663448, 00691812663387
- Basic UDI-DI
- 4030457-FinnCo-001-MN
- Direct Marketing DI
- 0069181266339400691812663479006918126634000069181266342400691812663417006918126634550069181266343100691812663370006918126634620069181266344800691812663387
- 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