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RapidFor™

by Vitrosens Biotechnology Inc. Türkiye EUDAMED

Ref VMD166TD, VMD166

EMDN W0105040616

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD Number868499827VMD166TDPL Basic UDI-DIDate9 Sep 2026RegisteredStatusActive
European UnionCE/IVDR Number868499827VMD166TDPL Basic UDI-DIDate9 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDD, CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Norovirus v2.0 Test Kit
Model / Reference
VMD166TD, VMD166
Primary DI / UDI-DI
08684998272032
Basic UDI-DI
868499827VMD166TDPL, B-08684998272032
EMDN Code
W0105040616 Norovirus
Device Class
Class B
Class IVD General
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 08684998272032|868499827VMD166TDPL 61 fields · synced 24 Oct 2026
  • EUDAMED 08684998272032|B-08684998272032 61 fields · synced 24 Oct 2026