Suitcase bi-folding wheelchair ramp
by Wonsh Ramp Industry Co., Limited 4 variants
Ref 80-10001Model WR80100; WR80101; WR80102; WR80103
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 | Number698031869ER407MFN 06980318690022 | Date28 Sep 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- Withdrawn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
- Suitcase bi-folding wheelchair ramp
- Model / Reference
- WR80100, WR80101, WR80102, WR80103, 80-10001
- Primary DI / UDI-DI
- 06980318690022
- Basic UDI-DI
- 698031869ER407MFN
- EMDN Code
- Y183015 Portable ramps
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000058395
- Authorised representative
- HUMISS TRADING S. L. ES-AR-000040177
Other devices from Wonsh Ramp Industry Co., Limited
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