Lidergrip 20/1
Ref 0021605Model VENDAJE TUBULAR COMPRESIVO
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 | Number18426716LGRIP01QQ 08426716216054 | Date3 Mar 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- Withdrawn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
- Lidergrip
- Model / Reference
- VENDAJE TUBULAR COMPRESIVO, 0021605
- Primary DI / UDI-DI
- 08426716216054
- Basic UDI-DI
- 18426716LGRIP01QQ
- Direct Marketing DI
- 08426716216054
- EMDN Code
- M030499 Elastic bandages, support and compression - other
- Device Class
- Class I
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- ES-MF-000004664
Other devices from Lidermed S.A.
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