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Klinidur ® cohesive bandage

EUDAMED

Class I (EU MDR)

Ref 4051 1803Ref 4051 1804

by FARMABAN s.a.

Identity

Trade Name
Klinidur ® cohesive bandage EUDAMED
Device Name
Venda elástica cohesiva de compresión EUDAMED
Model / Reference
4051 1803 EUDAMED
4051 1804 EUDAMED

Identifiers

Primary DI / UDI-DI
08428012302486 EUDAMED
08428012302493 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 (2)

  • EUDAMED 3f240a34-a8d1-4a13-920a-5163523350f3 61 fields · synced Jul 16, 2026
  • EUDAMED a53dd9e4-f0b5-40a8-9726-d9b9c351a2de 61 fields · synced May 18, 2026