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RapidFor™

by Vitrosens Biotechnology Inc. 280 variants

Ref VMD36, VMD36STS01Model VMD36DTS, VMD36STS

RapidFor™ (VMD36) is a device classified as IVD General (EU), Class B (EU) made by Vitrosens Biotechnology Inc., registered in EUDAMED on 15 Sep 2026 (Basic UDI-DI B-08684998273923), active as of 25 Oct 2026.

Active European Union

CE IVDR CE IVDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberB-08684998273923 Basic UDI-DI Date15 Sep 2026RegisteredStatusActive
European UnionCE/IVDD NumberB-08684998273923 Basic UDI-DI Date15 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR, CE/IVDD Active

Specification

EUDAMED

Device name
Strep A Test Kit
Model / reference
VMD36DTS, VMD36, VMD36STS01, VMD36STS
Primary DI / UDI-DI
08684998273923, 08684595033944, 08684998273718
Basic UDI-DI
B-08684998273923, 868499827VMD36STSVL, B-08684595033944, B-08684998273718
EMDN code
W0105090103 Strep. a - rt & poc
Device class
Class IVD General
Class B
EU registration type
Legacy device (under a directive)
Standard device
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000026452

Similar devices in this category

Other devices filed under STREP. A - RT & POC.

Other devices from Vitrosens Biotechnology Inc.

See all devices from Vitrosens Biotechnology Inc. →

Properties

  • Reagent
  • IVD kit
  • Professional testing
Other properties (10, all answered No)