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Rayvolve

EUDAMED

Class IIa (EU MDR)

Ref Rayvolve - Full cloud (Version 5)

by AZmed

Identity

Trade Name
Rayvolve EUDAMED
Device Name
Rayvolve EUDAMED
Model / Reference
Rayvolve - Full cloud (Version 5) EUDAMED

Identifiers

Primary DI / UDI-DI
37700180711072 EUDAMED
Basic UDI-DI
3770018071008VP EUDAMED
Direct Marketing DI
37700180711072 EUDAMED
EMDN Code
Z11060292 DIGITAL COMPUTED RADIOGRAPHY (CR) SYSTEMS - MEDICAL DEVICE SOFTWARE 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 b935954e-0132-416c-92bb-6a920617bd31 61 fields · synced May 23, 2026