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Fuji Medical Dry Imaging Film

EUDAMED

Class I (EU MDR)

Ref 4741028223

by FUJIFILM Corporation

Identity

Trade Name
Fuji Medical Dry Imaging Film EUDAMED
Device Name
Fuji Medical Dry Imaging Film EUDAMED
Model / Reference
4741028223 EUDAMED

Identifiers

Primary DI / UDI-DI
04547410282238 EUDAMED
Basic UDI-DI
454741010100000000000002Y EUDAMED
Unit of Use DI
84547410282234 EUDAMED
EMDN Code
Z130107 FILMS FOR REPRODUCTION FROM LASER TECHNOLOGIES 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

Fuji Medical Dry Imaging Film by FUJIFILM Corporation — 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

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

Sources (1)

  • EUDAMED 1ede0dc9-aeeb-435b-b544-671ea59d6c1e 61 fields · synced Jun 19, 2026