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méditech

EUDAMED

Class I (EU MDR)

Ref SO1003

by FARMABAN s.a.

Identity

Trade Name
méditech EUDAMED
Device Name
ESPARADRAPO ELÁSTICO ADHESIVO EUDAMED
Model / Reference
SO1003 EUDAMED

Identifiers

Primary DI / UDI-DI
08428012302615 EUDAMED
Basic UDI-DI
8428012VEAN104QJ EUDAMED
EMDN Code
M03030199,M03040199,M03040299 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

méditech by FARMABAN 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
FARMABAN s.a.
EUDAMED SRN
ES-MF-000004713

Sources (1)

  • EUDAMED c604fe70-5906-4fbd-b355-f2a574f374a6 61 fields · synced Jun 17, 2026