FinnComfort
by Waldi Schuhfabrik GmbH 1,000+ variants
Ref 01363-902979
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- Withdrawn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
- 01363-902979
- Primary DI / UDI-DI
- 04030457541197, 04030457541166, 04030457541142, 04030457541128, 04030457541098, 04030457541135, 04030457541104, 04030457541111, 04030457541159, 04030457541180, 04030457541173
- Basic UDI-DI
- 4030457-FinnCo-001-MN
- Direct Marketing DI
- 0403045754119704030457541166040304575411420403045754112804030457541098040304575411350403045754110404030457541111040304575411590403045754118004030457541173
- 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