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Intraskan Dc and It's Variants

by Skanray Technologies Private Limited EUDAMED

Active European Union

Ref 303-000134 -18

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number890426940100173 Basic UDI-DIDate30 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Intraskan Dc and It's Variants
Model / Reference
303-000134 -18
Primary DI / UDI-DI
08904269400507
Basic UDI-DI
890426940100173
Direct Marketing DI
08904269400507
EMDN Code
Z1103040102 Equipment for digital endoral radiology
Device Class
Class IIb
Market of Registration
Belgium

Manufacturer details

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

Other devices from Skanray Technologies Private Limited

See all devices from Skanray Technologies Private Limited →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No