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Dräger DrugTest 5000

by Dräger Safety AG & Co. KGaA Germany EUDAMED

Ref 8323646 EMDN W0102090102,W0102090104,W0102090105,W0102090106,W0102090110,W0102090113,W0102090199

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-04048675682776 Basic UDI-DIDate5 Nov 2025RegisteredStatusActive

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  • Withdrawn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 24 Oct 2026

Device Name
Dräger DrugTest 5000 STK 8
Model / Reference
8323646
Primary DI / UDI-DI
04048675682776
Basic UDI-DI
B-04048675682776
EMDN Code
W0102090102,W0102090104,W0102090105,W0102090106,W0102090110,W0102090113,W0102090199
Device Class
Class IVD General
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000014172

Other devices from Dräger Safety AG & Co. KGaA

See all devices from Dräger Safety AG & Co. KGaA →

Properties & raw data

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

Sources (1)

  • EUDAMED fc3497b8-961f-4409-acb1-4ac0952e2ff5 61 fields · synced 24 Oct 2026