FinnComfort
by Waldi Schuhfabrik GmbH 1,000+ variants
Ref 01362-322046
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- Withdrawn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
- 01362-322046
- Primary DI / UDI-DI
- 04030457566756, 04030457566701, 04030457566732, 04030457566671, 04030457566664, 04030457566657, 04030457566718, 04030457566725, 04030457566749, 04030457566688, 04030457566695
- Basic UDI-DI
- 4030457-FinnCo-001-MN
- Direct Marketing DI
- 0403045756675604030457566701040304575667320403045756667104030457566664040304575666570403045756671804030457566725040304575667490403045756668804030457566695
- 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