Lidergrip

by Lidermed S.A. 21 variants

Ref 002082Model VENDAJE TUBULAR COMPRESIVO

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number18426716LGRIP01QQ Basic UDI-DI 08426716208028UDI-DI	Date3 Mar 2026Registered	StatusActive

Official records

EUDAMED public site Basic UDI-DI 18426716LGRIP01QQ — open Devices and search for it

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference: VENDAJE TUBULAR COMPRESIVO, 002082

Primary DI / UDI-DI: 08426716208028
Basic UDI-DI: 18426716LGRIP01QQ
Direct marketing DI: 08426716208028
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: Spain

Manufacturer details

EUDAMED SRN: ES-MF-000004664

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Properties

Contains latex

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