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AESKUBLOTS® Food Intolerance TWO

by Aesku.Diagnostics GmbH & Co. KG FDA registration: Germany EUDAMED

Ref 431402 EMDN W0102010106

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-04250289510585 Basic UDI-DIDate5 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
AESKUBLOTS® Food Intolerance
Model / Reference
431402
Primary DI / UDI-DI
04250289510585
Basic UDI-DI
B-04250289510585
EMDN Code
W0102010106 Immunoglobulin g subclass reagents
Device Class
Class IVD General
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000026925

Other devices from AESKU.DIAGNOSTICS GmbH&Co.KG

See all devices from AESKU.DIAGNOSTICS GmbH&Co.KG →

Properties & raw data

Show properties, registry sources and raw records
  • Human Tissues
  • Animal Tissues
  • Microbial Substances
  • Professional Testing
Other properties (6)
  • Sterile: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No

Sources (1)

  • EUDAMED 26409cd7-26fd-4e18-a260-24ae825636af 61 fields · synced 23 Oct 2026