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RapidFor™

by Vitrosens Biotechnology Inc. 73 variants

Ref CFP87P50, PCR87

RapidFor™ (CFP87P50) is a device classified as Class B (EU), IVD General (EU) made by Vitrosens Biotechnology Inc., registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 868511580PCR87JY), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD Number868511580PCR87JY Basic UDI-DI 08684595033258UDI-DIDate2 Nov 2026RegisteredStatusActive
European UnionCE/IVDR Number868511580PCR87JY Basic UDI-DI 08684595033258UDI-DIDate2 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD, CE/IVDR Active

Specification

EUDAMED

Trade name
RapidFor™
ChainFor™
Device name
Strep A qPCR Kit
Model / reference
CFP87P50, PCR87
Primary DI / UDI-DI
08684595033258
Basic UDI-DI
868511580PCR87JY, B-08684595033258
EMDN code
W0105011103 Strep. a detection by na reagents
Device class
Class B
Class IVD General
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000026452

Similar devices in this category

Other devices filed under STREP. A DETECTION BY NA REAGENTS.

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)