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Drystar Dt 2 Mammo

EUDAMED

Class I (EU MDR)

Ref 5VCEORef 5VCDM

by Agfa NV

Identity

Trade Name
DRYSTAR DT 2 MAMMO EUDAMED
Device Name
Hard Copy Film EUDAMED
Model / Reference
5VCEO EUDAMED
5VCDM EUDAMED

Identifiers

Primary DI / UDI-DI
05414904128336 EUDAMED
05414904128367 EUDAMED
Basic UDI-DI
5414904273005XE EUDAMED
Unit of Use DI
05414904226797 EUDAMED
05414904226810 EUDAMED
EMDN Code
Z130106 DRY THERMAL PRINTER X-RAY FILMS 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

Drystar Dt 2 Mammo 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 (2)

  • EUDAMED 032f1732-b20a-45be-9375-fa903c877325 61 fields · synced Jul 9, 2026
  • EUDAMED 7b37d544-bf37-407f-8f2e-f7dbbf02de66 61 fields · synced May 19, 2026