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Rayscan

by AZmed 3 variants

Part of a family of 20 devices: see the family page

Ref Rayscan- On premise ( Version 1)

Rayscan is a medical device (EU MDR Class IIa; EMDN category computed tomographs (ct) - medical device software) made by Azmed Sas, registered in EUDAMED on 30 Mar 2023 (Basic UDI-DI 3770018071008VP), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3770018071008VP Basic UDI-DI 37700180711690UDI-DIDate30 Mar 2023RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Rayvolve
Model / reference
Rayscan- On premise ( Version 1)
Primary DI / UDI-DI
37700180711690
Basic UDI-DI
3770018071008VP
Direct marketing DI
37700180711690
EMDN code
Z11030692 Computed tomographs (CT) - medical device software
Device class
Class IIa
Special device type
Software
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000014277

Similar devices in this category

Other devices filed under COMPUTED TOMOGRAPHS (CT) - MEDICAL DEVICE SOFTWARE.

Other devices from Azmed Sas

  • Rayvolve

    Class IIa

  • Rayvolve V 6

    Class II

  • Rayscan

    Class IIa

  • Rayvolve 4

    Class II

See all devices from Azmed Sas →

Properties

Other properties (14, all answered No)