Achillodyn
Ref 07071
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 | Number04029925Y06120601V7 | Date16 Oct 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- Withdrawn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
- Device Name
- Swede-O-Universal
- Model / Reference
- 07071
- Primary DI / UDI-DI
- 04029925010648, 04029925140888, 04029925240823, 04029925100660, 04029925240830, 04029925010631, 04029925140918, 04029925003602, 04029925003640, 04029925140895, 04029925100684, 04029925100677, 04029925010600, 04029925003626, 04029925010617, 04029925003633, 04029925140871, 04029925140901, 04029925240854, 04029925100707, 04029925100691, 04029925003619, 04029925010624
- Basic UDI-DI
- 04029925Y06120601V7
- EMDN Code
- Y06120601 Passive ankle-foot orthoses
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000006346
Other devices from SPORLASTIC GMBH & Co.KG
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: 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