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Drystar Dt 5 Mammo

EUDAMED

Class I (EU MDR)

Ref 51BQFRef 51BSKRef 51BRH

by Agfa NV

Identity

Trade Name
DRYSTAR DT 5 MAMMO EUDAMED
Device Name
Hard Copy Film EUDAMED
Model / Reference
51BQF EUDAMED
51BSK EUDAMED
51BRH EUDAMED

Identifiers

Primary DI / UDI-DI
05414904175712 EUDAMED
05414904175736 EUDAMED
05414904175729 EUDAMED
Basic UDI-DI
5414904273005XE EUDAMED
Unit of Use DI
05414904229637 EUDAMED
05414904229590 EUDAMED
05414904229613 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 5 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 (3)

  • EUDAMED 64f46ee3-5f9c-4d41-af30-9a997369b06a 61 fields · synced Sep 30, 2026
  • EUDAMED 326e05e7-eb2b-4b37-b8cb-df959a8741a1 61 fields · synced May 18, 2026
  • EUDAMED b716173f-0896-4e17-8509-3c2a10481bb5 61 fields · synced May 19, 2026