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FUJI Medical X-ray Film

EUDAMED

Class IIa (EU MDR)

Ref 4741019233

by FUJIFILM Corporation

Identity

Trade Name
FUJI Medical X-ray Film EUDAMED
Device Name
FUJI Medical X-ray Film EUDAMED
Model / Reference
4741019233 EUDAMED

Identifiers

Primary DI / UDI-DI
04547410192339 EUDAMED
Basic UDI-DI
4547410101000000000000132 EUDAMED
Unit of Use DI
84547410192335 EUDAMED
EMDN Code
Z130101 GENERAL PURPOSE X-RAY FILMS EUDAMED

Classification

Device Class
Class IIa 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

FUJI Medical X-ray Film by FUJIFILM Corporation — Class IIa — 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

EUDAMED SRN
JP-MF-000010401
Authorised Representative
FUJIFILM Healthcare Europe GmbH DE-AR-000040920

Sources (1)

  • EUDAMED cac27585-cb8f-4227-8275-413edad8f96a 61 fields · synced Jun 15, 2026