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RapidFor™

by Vitrosens Biotechnology Inc. Türkiye EUDAMED

Ref VMD42Model VMD42TD EMDN W0105040629

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberB-08683347941483 Basic UDI-DIDate8 Sep 2026RegisteredStatusActive
European UnionCE/IVDD NumberB-08683347941483 Basic UDI-DIDate8 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR, CE/IVDD Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Astrovirus Test Kit
Model / Reference
VMD42TD, VMD42
Primary DI / UDI-DI
08683347941483
Basic UDI-DI
B-08683347941483, 868334794VMD42TD3Y
EMDN Code
W0105040629 Astrovirus
Device Class
Class IVD General
Class B
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000026452

Other devices from Vitrosens Biotechnology Inc.

See all devices from Vitrosens Biotechnology Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Reagent
  • Professional Testing
Other properties (9)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (2)

  • EUDAMED 2a0a2e46-f9e4-4290-842a-4699bc33d702 61 fields · synced 23 Oct 2026
  • EUDAMED 08683347941483|868334794VMD42TD3Y 61 fields · synced 24 Oct 2026