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RapidFor™

by Vitrosens Biotechnology Inc. Türkiye EUDAMED

Ref VMD140Model VMD140FD

EMDN W0105040617

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberB-08685260610897 Basic UDI-DIDate21 Oct 2026RegisteredStatusActive
European UnionCE/IVDD NumberB-08685260610897 Basic UDI-DIDate21 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR, CE/IVDD Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
hMPV Test Kit
Model / Reference
VMD140FD, VMD140
Primary DI / UDI-DI
08685260610897
Basic UDI-DI
B-08685260610897, 868459503VMD140SC9C
EMDN Code
W0105040617 Human metapneumovirus
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 08685260610897|B-08685260610897 61 fields · synced 24 Oct 2026
  • EUDAMED 08685260610897|868459503VMD140SC9C 61 fields · synced 24 Oct 2026