Tendrex
by Sanita Consumer Products 7 variants
Ref UP050517
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 | Number5281001431337QY 5281001431337 | Date18 Aug 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- Withdrawn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
- UP Tendrex 40X60CM 25X6
- Model / Reference
- UP050517
- Primary DI / UDI-DI
- 5281001431337
- Basic UDI-DI
- 5281001431337QY
- EMDN Code
- T04010201 Untuckable underpads
- Device Class
- Class I
- EU market of registration
- Hungary
Manufacturer details
- EUDAMED SRN
- EG-MF-000057771
- Authorised representative
- EUROMED Authorized Services Kft HU-AR-000051628
Other devices from Sanita Consumer Products
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