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Cawo Dry Mammo Film

EUDAMED

Class I (EU MDR)

Ref 59CM8Ref XCMX3

by Agfa NV

Identity

Trade Name
CAWO DRY MAMMO FILM EUDAMED
Device Name
Hard Copy Film EUDAMED
Model / Reference
59CM8 EUDAMED
XCMX3 EUDAMED

Identifiers

Primary DI / UDI-DI
05414904220535 EUDAMED
05414904236376 EUDAMED
Basic UDI-DI
5414904273005XE EUDAMED
Unit of Use DI
05414904220542 EUDAMED
05414904236383 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

Cawo Dry Mammo Film by Agfa NV — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Manufacturer's product page: Dry Digital Film

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 0b79d0b8-8b36-468b-a704-e582c68bb0af 61 fields · synced Jul 9, 2026
  • EUDAMED c05d784c-2a80-44b8-b8f2-d627dcc6ae6a 61 fields · synced May 18, 2026