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Prone Breast Board

EUDAMED

Class I (EU MDR)

Ref 70-100Model Prone Breast Board

by Aktina Medical Corp

Identity

Trade Name
Prone Breast Board EUDAMED
Device Name
SenoView Prone Breast Board EUDAMED
Model / Reference
Prone Breast Board EUDAMED
70-100 EUDAMED

Identifiers

Primary DI / UDI-DI
+B365701000 EUDAMED
Basic UDI-DI
++B36570100FM EUDAMED
Direct Marketing DI
+B365701000 EUDAMED
EMDN Code
Z11010199 LINEAR ACCELERATORS – OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Prone Breast Board by Aktina Medical Corp — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Manufacturer's product page: SenoView Prone Breast

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Aktina Medical Corp
EUDAMED SRN
US-MF-000005935
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED f45de795-5247-42dc-b50a-5793340db661 61 fields · synced May 22, 2026