Hekagrip Size E
Ref OT0922-1Model VENDAJE TUBULAR COMPRESIVO
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number18426716LGRIP01QQ 08426716221058 | Date3 Mar 2026 | StatusActive |
Official records
- EUDAMED public site 18426716LGRIP01QQ
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- Withdrawn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, OT0922-1
- Primary DI / UDI-DI
- 08426716221058
- Basic UDI-DI
- 18426716LGRIP01QQ
- Direct marketing DI
- 08426716221058
- EMDN code
- M030499 Elastic bandages, support and compression - other
- Device class
- Class I
- System or procedure pack
- Procedure pack which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- ES-MF-000004664
Other devices from Lidermed S.A.
Properties
Other properties (13)
- Supplied sterile: No
- Sterilise before use: No
- Implantable: No
- Reusable: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No