FinnComfort
by Waldi Schuhfabrik GmbH 1,000+ variants
Ref 82519-845404
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- Withdrawn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
- 82519-845404
- Primary DI / UDI-DI
- 04030457527566, 04030457527610, 04030457527597, 04030457527627, 04030457527580, 04030457527634, 04030457527641, 04030457527603, 04030457527573, 04030457527658
- Basic UDI-DI
- 4030457-FinnCo-001-MN
- Direct Marketing DI
- 04030457527566040304575276100403045752759704030457527627040304575275800403045752763404030457527641040304575276030403045752757304030457527658
- 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