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IMMULITE 2000 Micropolyspora faeni Specific Allergen

by Siemens Healthcare Diagnostics Products Ltd. FDA registration: Germany EUDAMED

Ref 10386025Model IVDR_67_LLB_DUB-C_B_REAG_Micropolyspora faeni Spfc Algn EMDN W01020202

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number0405686900515V9 Basic UDI-DIDate11 Jun 2026RegisteredStatusActive

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  • Withdrawn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 25 Oct 2026

Device Name
IVDR_67_LLB_DUB-C_B_REAG_Micropolyspora faeni Spfc Algn
Model / Reference
IVDR_67_LLB_DUB-C_B_REAG_Micropolyspora faeni Spfc Algn, 10386025
Primary DI / UDI-DI
00630414995908
Basic UDI-DI
0405686900515V9
EMDN Code
W01020202 Immunoglobulin e - specific, monotest/monoresult
Device Class
Class B
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
GB-MF-000016339
Authorised representative
Siemens Healthcare Diagnostics Manufacturing Limited IE-AR-000006763

Other devices from Siemens Healthcare Diagnostics Products Limited

See all devices from Siemens Healthcare Diagnostics Products Limited →

Properties & raw data

Show properties, registry sources and raw records
  • Animal Tissues
  • Microbial Substances
  • Reagent
  • Professional Testing
Other properties (7)
  • Sterile: No
  • Human Tissues: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 00630414995908|0405686900515V9 61 fields · synced 25 Oct 2026