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Drystar Dt 10 Mammo

EUDAMED

Class I (EU MDR)

Ref 51BJZRef 51BHX

by Agfa NV

Identity

Trade Name
DRYSTAR DT 10 MAMMO EUDAMED
Device Name
Hard Copy Film EUDAMED
Model / Reference
51BJZ EUDAMED
51BHX EUDAMED

Identifiers

Primary DI / UDI-DI
05414904175644 EUDAMED
05414904175637 EUDAMED
Basic UDI-DI
5414904273005XE EUDAMED
Unit of Use DI
05414904229774 EUDAMED
05414904229798 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 10 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 81908f0e-c9aa-46a3-86b6-7d7d91aa4bc4 61 fields · synced Jul 12, 2026
  • EUDAMED 06ca551f-d105-4f4e-80b5-256faddb3ee6 61 fields · synced May 11, 2026