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Fuller Laboratories by VMRD Francisella tularensis and Brucella abortus MIF IgG Antibody Kit

by VMRD, Inc. United States EUDAMED

Ref FTG-120

EMDN W0105011799

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-00850078245175 Basic UDI-DIDate11 Jun 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
Francisella tularensis and Brucella abortus MIF IgG Antibody Kit
Model / Reference
FTG-120
Primary DI / UDI-DI
00850078245175
Basic UDI-DI
B-00850078245175
EMDN Code
W0105011799 Bacteriology immunoassay - other
Device Class
Class IVD General
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
US-MF-000049394
Authorised representative
MediMark Europe Sarl. FR-AR-000000182

Other devices from VMRD, Inc.

See all devices from VMRD, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Animal Tissues
  • Microbial Substances
  • Professional Testing
Other properties (7)
  • Sterile: No
  • Human Tissues: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No

Sources (1)

  • EUDAMED 4d180e3d-ce64-46c1-beec-b689ce19052a 61 fields · synced 22 Oct 2026