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Lidergrip Embo

EUDAMED

Class I (EU MDR)

Ref 0021206Model VENDAJE TUBULAR COMPRESIVO

by Lidermed S.a.

Identity

Trade Name
LIDERGRIP EMBO EUDAMED
Device Name
LIDERGRIP EUDAMED
Model / Reference
VENDAJE TUBULAR COMPRESIVO EUDAMED
0021206 EUDAMED

Identifiers

Primary DI / UDI-DI
08426716212063 EUDAMED
Basic UDI-DI
18426716LGRIP01QQ EUDAMED
Direct Marketing DI
08426716212063 EUDAMED
EMDN Code
M030405 COMPRESSION STOCKINGS 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

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

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 5189a3e1-cc56-4b9e-97c0-726c4bf8b8a9 61 fields · synced Jun 20, 2026