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Klinidur® cohesive bandage

EUDAMED

Class I (EU MDR)

Ref 40511802

by FARMABAN s.a.

Identity

Trade Name
Klinidur® cohesive bandage EUDAMED
Device Name
Venda elástica cohesiva de compresión EUDAMED
Model / Reference
40511802 EUDAMED

Identifiers

Primary DI / UDI-DI
08428012302479 EUDAMED
Basic UDI-DI
8428012COMPRESIONTCUJ EUDAMED
EMDN Code
M0304010201 ELASTIC COMPRESSION BANDAGES, COHESIVE, LOW EXTENSIBILITY (<70%) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Klinidur® cohesive bandage 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 c2a4aefd-425e-4794-acc0-118a235ae1c6 61 fields · synced Jun 18, 2026