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DyoniFOB

by Dyonmed SA Greece EUDAMED

Ref DNGL101, DNCT102

EMDN W0102039013

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-05200251201200 Basic UDI-DIDate13 Nov 2023RegisteredStatusActive

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

Trade Name
DyoniFOB
DyoniFOB Combo T
Model / Reference
DNGL101, DNCT102
Primary DI / UDI-DI
05200251201200, 05200251204102
Basic UDI-DI
B-05200251201200, B-05200251204102
EMDN Code
W0102039013 Fecal occult blood (ic)
Device Class
Class IVD General
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000033588

Other devices from Dyonmed SA

See all devices from Dyonmed SA →

Properties & raw data

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

Sources (2)

  • EUDAMED 44fee23d-ea97-4ce8-9ccf-5857cc89309d 61 fields · synced 22 Oct 2026
  • EUDAMED 05200251204102|B-05200251204102 61 fields · synced 18 May 2026