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Liderfix

EUDAMED

Class I (EU MDR)

Ref 0030402Model VENDAJE TUBULAR DE MALLA

by Lidermed S.a.

Identity

Trade Name
LIDERFIX EUDAMED
Device Name
LIDERFIX EUDAMED
Model / Reference
VENDAJE TUBULAR DE MALLA EUDAMED
0030402 EUDAMED

Identifiers

Primary DI / UDI-DI
08426716304027 EUDAMED
Basic UDI-DI
18426716LDFIX01LM EUDAMED
Direct Marketing DI
08426716304027 EUDAMED
EMDN Code
M03030103 TUBULAR NET BANDAGES 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

Yes

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

Liderfix 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 2eccf032-1289-4ae4-9d2d-f5a2dc44d0bd 61 fields · synced Jun 19, 2026