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RapidFor™ Mycoplasma pneumoniae Ab Rapid Test Kit

by Vitrosens Biotechnology Inc. Türkiye EUDAMED

Ref VMD65 EMDN W0105010802

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-08683548250773 Basic UDI-DIDate7 Mar 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Mycoplasma pneumoniae Ab Rapid Test Kit
Model / Reference
VMD65
Primary DI / UDI-DI
08683548250773
Basic UDI-DI
B-08683548250773
EMDN Code
W0105010802 Mycoplasma antibody assays
Device Class
Class IVD General
Market of Registration
Germany

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
  • Near-Patient Testing
  • Professional Testing
  • Companion Diagnostics
Other properties (6)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Surgical Instrument: No

Sources (1)

  • EUDAMED 1b04df09-6cd3-40d2-9e18-946da7f26cfc 61 fields · synced 22 Oct 2026