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Platelia Aspergillus IgG

by Bio-Rad

Ref 62783

Platelia Aspergillus IgG (62783) is a Class C device made by Bio-Rad, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 361052A000197Q), active as of 7 Nov 2026.

Active European Union

CE IVDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number361052A000197Q Basic UDI-DI 03610520002469UDI-DIDate30 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device name
EIA Microplate Aspergillus IgG
Model / reference
62783
Primary DI / UDI-DI
03610520002469
Basic UDI-DI
361052A000197Q
EMDN code
W0105060301 Aspergillus
Device class
Class C
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000006261

Similar devices in this category

Other devices filed under MYCOLOGY IMMUNOASSAYS.

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Properties

  • Contains human tissues or cells
  • Contains animal tissues or cells
  • Contains substances of microbial origin
  • Reagent
  • IVD kit
  • Professional testing
Other properties (7, all answered No)