← Back to catalogue

Lidergrip 20/1

EUDAMED

Class I (EU MDR)

Ref 0021608Model VENDAJE TUBULAR COMPRESIVO

by Lidermed S.a.

Identity

Trade Name
LIDERGRIP 20/1 EUDAMED
Device Name
LIDERGRIP EUDAMED
Model / Reference
VENDAJE TUBULAR COMPRESIVO EUDAMED
0021608 EUDAMED

Identifiers

Primary DI / UDI-DI
08426716216085 EUDAMED
Basic UDI-DI
18426716LGRIP01QQ EUDAMED
Direct Marketing DI
08426716216085 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 20/1 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 94f59f4f-0a7c-450d-93e5-9e950553814f 61 fields · synced Jul 15, 2026