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LIOFeron® TB/LTBI

by Lionex GmbH Germany EUDAMED

Ref LIOFeron 01_22 EMDN W01030601

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberPP07924LIOFERON0122 Basic UDI-DIDate15 Sep 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
LIOFeron® HUMAN BLOOD STIMULATION TUBES
Model / Reference
LIOFeron 01_22
Primary DI / UDI-DI
111761298322
Basic UDI-DI
PP07924LIOFERON0122
EMDN Code
W01030601 INTERFERONS (α, β, ɣ…)
Device Class
Class C
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000038504

From the manufacturer

Manufacturer's product page: LIOFeron® TB/LTBI

Other devices from Lionex GmbH

Properties & raw data

Show properties, registry sources and raw records
  • Microbial Substances
  • Professional Testing
Other properties (9)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED a85310ad-7846-4c6e-92ef-3d51e3a3c814 61 fields · synced 24 Oct 2026