Skip to content

RapidFor™

by Vitrosens Biotechnology Inc. Türkiye EUDAMED

Ref VMPO126Model VMPO126UP EMDN W0105090109

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberB-08684998271882 Basic UDI-DIDate26 Aug 2026RegisteredStatusActive
European UnionCE/IVDD NumberB-08684998271882 Basic UDI-DIDate26 Aug 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  • Withdrawn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 23 Oct 2026

Device Name
S. pneumonia (FIA)
Model / Reference
VMPO126UP, VMPO126
Primary DI / UDI-DI
08684998271882
Basic UDI-DI
B-08684998271882, 868499827VMPO126UPL4
EMDN Code
W0105090109 Strep. pneumoniae - rt & poc
Device Class
Class IVD General
Class C
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 d023efd6-db41-43b1-94fa-9d1cfedce587 61 fields · synced 23 Oct 2026
  • EUDAMED 08684998271882|868499827VMPO126UPL4 61 fields · synced 15 Oct 2026