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LDBIO TOXO II IgG

by Ldbio Diagnostics 3 variants

Ref TOXO II 12G

Active European Union

CE IVDR CE IVDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD Number3770027793WBT2G7F Basic UDI-DI Date18 Sep 2026RegisteredStatusActive
European UnionCE/IVDR Number3770027793WBT2G7F Basic UDI-DI Date18 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD, CE/IVDR Active

Specification

EUDAMED

Model / Reference
TOXO II 12G
Primary DI / UDI-DI
37700277931994, D-37700277931992V
Basic UDI-DI
3770027793WBT2G7F, B-37700277931992V
EMDN Code
W0105050102 Toxoplasma antibody igg
Device Class
Class C
Class IVD Annex II List B
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000021697

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Properties

  • Human Tissues
  • Animal Tissues
  • Reagent
  • Professional Testing

Other properties (7)

  • Sterile: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No