Loop SORG
by SORG Rollstuhltechnik GmbH & Co.KG
Ref 802
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 | Number426073765100TIL100XXXX63 04260737650060 | Date16 Apr 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- Withdrawn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
- Kantelrollstühle
- Model / Reference
- 802
- Primary DI / UDI-DI
- 04260737650060
- Basic UDI-DI
- 426073765100TIL100XXXX63
- Direct Marketing DI
- 04260737650060
- EMDN Code
- Y122103 Push wheelchairs
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000008366
From the manufacturer
Manufacturer's product page: LoopSORG
Other devices from SORG Rollstuhltechnik 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