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FUJI Medical X-ray Film

by FUJIFILM Corporation Japan EUDAMED

Ref 4741019292

EMDN Z130101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4547410101000000000000132 Basic UDI-DIDate25 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 4203162CE01 Amended

    Quality management system EU MDR

    Notified body
    Notified body 0344
    Issued
    15 Jul 2024
    Expires
    27 Jun 2029
    Reason
    Mnf ar change

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
4741019292
Primary DI / UDI-DI
04547410192926
Basic UDI-DI
4547410101000000000000132
Unit of Use DI
84547410192922
EMDN Code
Z130101 General purpose x-ray films
Device Class
Class IIa
Market of Registration
Netherlands

Manufacturer details

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

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED bd1a1841-5035-4cf6-9bb8-4118e926359a 61 fields · synced 22 Oct 2026