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Prostatic Acid Phosphatase (PAP) Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay）

by Biobase Diagnostic Technology (Shandong) Co., Ltd. China EUDAMED

Ref 200 Tests/kit（DR1157-3）Model 200 Tests/kit EMDN W0102030120

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-06974969982964 Basic UDI-DIDate6 May 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  • Withdrawn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 24 Oct 2026

Model / Reference
200 Tests/kit, 200 Tests/kit（DR1157-3）
Primary DI / UDI-DI
06974969982964
Basic UDI-DI
B-06974969982964
EMDN Code
W0102030120 Prostatic acid phosphatase (ic)
Device Class
Class IVD General
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000025964
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

Other devices from Biobase Diagnostic Technology (Shandong) Co., Ltd.

See all devices from Biobase Diagnostic Technology (Shandong) Co., Ltd. →

Properties & raw data

Show properties, registry sources and raw records
  • Reagent
  • Professional Testing
Other properties (8)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No

Sources (1)

  • EUDAMED 76f186aa-6d25-4271-a290-a219bf47f544 61 fields · synced 24 Oct 2026