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Lidergrip

EUDAMED

Class I (EU MDR)

Ref 0020408Model VENDAJE TUBULAR COMPRESIVO

by Lidermed S.a.

Identity

Trade Name
LIDERGRIP EUDAMED
Device Name
LIDERGRIP EUDAMED
Model / Reference
VENDAJE TUBULAR COMPRESIVO EUDAMED
0020408 EUDAMED

Identifiers

Primary DI / UDI-DI
08426716204082 EUDAMED
Basic UDI-DI
18426716LGRIP01QQ EUDAMED
Direct Marketing DI
08426716204082 EUDAMED
EMDN Code
M030499 ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Compression/pressure sock/stocking, reusable

Lidergrip by Lidermed S.a. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Lidermed S.a.
EUDAMED SRN
ES-MF-000004664

Sources (1)

  • EUDAMED eb1ddf23-787e-4a51-b0af-cce616793897 61 fields · synced Jun 19, 2026