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G334

EUDAMED

Class I (EU MDR)

Ref EKNCY

by Agfa NV

Identity

Trade Name
G334 EUDAMED
Device Name
Photochemicals EUDAMED
Model / Reference
EKNCY EUDAMED

Identifiers

Primary DI / UDI-DI
05414904030523 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

G334 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 7952c057-5d1a-440c-a4d0-e7eef3d61794 61 fields · synced Jun 19, 2026