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Skanmobile And Variants

EUDAMED

Class IIb (EU MDR)

Ref 303-000018-15

by Skanray Technologies Limited

Identity

Device Name
SKANMOBILE AND VARIANTS EUDAMED
Model / Reference
303-000018-15 EUDAMED

Identifiers

Primary DI / UDI-DI
08904269403669 EUDAMED
Basic UDI-DI
890426940100377 EUDAMED
Direct Marketing DI
08904269403669 EUDAMED
EMDN Code
Z11039016 MOBILE RADIOGRAPHIC UNITS EUDAMED

Classification

Device Class
Class IIb 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

Skanmobile And Variants by Skanray Technologies Limited — Class IIb — 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

EUDAMED SRN
IN-MF-000034819
Authorised Representative
SKANRAY EUROPE SRL IT-AR-000013034

Sources (1)

  • EUDAMED afac2999-bc0b-4613-957a-e93c6aad568f 61 fields · synced Jun 17, 2026