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G354

EUDAMED

Class I (EU MDR)

Ref EFBBM

by Agfa NV

Identity

Trade Name
G354 EUDAMED
Device Name
Photochemicals EUDAMED
Model / Reference
EFBBM EUDAMED

Identifiers

Primary DI / UDI-DI
05414904032909 EUDAMED
Basic UDI-DI
5414904272985ZC EUDAMED
EMDN Code
Z11079085 VARIOUS X-RAY FILM IMAGING SUPPORT INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

G354 by Agfa NV — 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

Manufacturer
Agfa NV
EUDAMED SRN
BE-MF-000000571

Sources (1)

  • EUDAMED cc788bc7-ce63-4129-95b7-ed4f760e6481 61 fields · synced Jun 18, 2026