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Mycoplasma Duo

by Bio-Rad United States EUDAMED

Ref 62740

EMDN W0104080207

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number361052A000187N Basic UDI-DIDate21 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Identification / Titration test for Mycoplasma
Model / Reference
62740
Primary DI / UDI-DI
03610520002407
Basic UDI-DI
361052A000187N
EMDN Code
W0104080207 Mycoplasma / ureaplasma - (incl. combined id-ast)
Device Class
Class C
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000006261

Other devices from Bio-Rad

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Properties & raw data

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

Sources (1)

  • EUDAMED 03610520002407|361052A000187N 61 fields · synced 24 Oct 2026