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Viseur AI

by Viseurai Saglik Ve Yapay Zeka Teknolojileri Anonim Sirketi 3 variants

Ref VSR.IMS.100

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number86853177211VIMSB4 Basic UDI-DI 08685317721118UDI-DIDate9 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Viseur AI IMS (Görüntü Yönetim Sistemi) / Viseur AI IMS (Image Management System)
Model / Reference
VSR.IMS.100
Primary DI / UDI-DI
08685317721118
Basic UDI-DI
86853177211VIMSB4
Direct Marketing DI
08685317721118
EMDN Code
W02079092 Various general purpose IVD instruments - IVD medical device software
Device Class
Class A
Special Device Type
Software
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000058625

Other devices from Viseurai Saglik Ve Yapay Zeka Teknolojileri Anonim Sirketi

Properties

  • Surgical Instrument

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • New Device: No