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Rayvolve

EUDAMED

Class IIa (EU MDR)

Ref Rayvolve- On premise (Version 4)

by AZmed

Identity

Trade Name
Rayvolve EUDAMED
Device Name
Rayvolve EUDAMED
Model / Reference
Rayvolve- On premise (Version 4) EUDAMED

Identifiers

Primary DI / UDI-DI
37700180710846 EUDAMED
Basic UDI-DI
3770018071008VP EUDAMED
Direct Marketing DI
37700180710846 EUDAMED
EMDN Code
Z11060282 DIGITAL COMPUTED RADIOGRAPHY (CR) SYSTEMS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
France 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

Rayvolve by AZmed — Class IIa — 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
AZmed
EUDAMED SRN
FR-MF-000014277

Sources (1)

  • EUDAMED 1e47897d-95da-4eab-b47c-ec63294f256b 61 fields · synced May 24, 2026