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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

0030401 — Class I MDR by LIDERMED S.A.

MD Atlas
LIDERMED S.A.

EUDAMED last updated this device on Mar 20, 2026

0030401

18426716LDFIX01LM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LIDERMED S.A.
UDI-DI code: 08426716304010
Reference / catalog number: 0030401

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Manufacturer information

Organization name: LIDERMED S.A.
SRN: ES-MF-000004664
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08426716304010
Basic UDI-DI: 18426716LDFIX01LM
Reference / catalog number: 0030401
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: LIDERFIX es un tejido tubular de malla que permite la sujeción de gasas y apósitos en diferentes partes del cuerpo como troncos, cabeza, brazos, piernas o dedos. se ajusta a la perfección a todas las partes de nuestro cuerpo sin oprimir. Su composición y diseño evitan que se formen pliegues tras su aplicación, así como también deslizamientos. Su aplicación y retirada son fáciles y sencillas. Está elaborado en material elástico que no genera deslizamientos en los nudos cuando este se somete a esfuerzos de tensión o cortes longitudinales o transversales causados durante el uso normal del mismo. Se puede cortar en cualquier parte de la venda tubular, sin miedo a desagarrarse o deshilacharse.
Additional information URL: https://www.lidermed.com/
Clinical sizes: Dedos gruesos, manos

EMDN nomenclature code(s)

M03030103TUBULAR NET BANDAGES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.