← Back to catalogue

Krepefix

EUDAMED

Class I (EU MDR)

Ref 1340

by FARMABAN s.a.

Identity

Trade Name
KREPEFIX EUDAMED
Device Name
KREPEFIX EUDAMED
Model / Reference
1340 EUDAMED

Identifiers

Primary DI / UDI-DI
08428012013405 EUDAMED
Basic UDI-DI
8428012COMPRESION6X EUDAMED
EMDN Code
M03030199,M03040299 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

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

Krepefix 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
FARMABAN s.a.
EUDAMED SRN
ES-MF-000004713

Sources (1)

  • EUDAMED 015b9627-e4d5-4506-85e4-a0fbdc3d6423 61 fields · synced Jun 20, 2026