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RapidFor™

by Vitrosens Biotechnology Inc. Türkiye EUDAMED

Ref VMD89Model VMD89TD

EMDN W0105011802

Regulatory status

as of 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-08683548254214 Basic UDI-DIDate8 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/IVDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
C.difficile Toxin A + B Test Kit
Model / Reference
VMD89TD, VMD89
Primary DI / UDI-DI
08683548254214
Basic UDI-DI
B-08683548254214, 868354825VMD89TD4Q
EMDN Code
W0105011802 C.difficile toxin a/b detection
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 bbe119c0-c4e3-40ed-b267-a82b70579ff7 61 fields · synced 22 Oct 2026
  • EUDAMED 08683548254214|868354825VMD89TD4Q 61 fields · synced 18 Oct 2026