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401y120038

EUDAMED

Class I (EU MDR)

Ref 04547410302769

by FUJIFILM Corporation

Identity

Trade Name
401Y120038 EUDAMED
Device Name
Shift Compression Plate EUDAMED
Model / Reference
04547410302769 EUDAMED

Identifiers

Primary DI / UDI-DI
04547410302769 EUDAMED
Basic UDI-DI
4547410101000000000008746 EUDAMED
EMDN Code
Z1103028099 MAMMOGRAPHY SYSTEMS - HARDWARE - OTHER 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

Category: Stationary mammographic x-ray system, digital

401y120038 by FUJIFILM Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Stationary mammographic x-ray system, digital.

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 d7ea2967-1426-45c8-a9c2-098119896dc6 61 fields · synced Jul 24, 2026