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BCR/ABL gene fusion detection kit

by Wuhan HealthCare Biotechnology Co., Ltd.

Ref FP-003

Active European Union

CE IVDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-697180825KCL003F3R5 Basic UDI-DI D-697180825KCL003F3R5UDI-DIDate5 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDD Active

Specification

EUDAMED

Device Name
BCR/ABL gene fusion detection kit
Model / Reference
FP-003
Primary DI / UDI-DI
D-697180825KCL003F3R5
Basic UDI-DI
B-697180825KCL003F3R5
EMDN Code
W01060208 T (9;22)
Device Class
Class IVD General
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
CN-MF-000033113
Authorised representative
Kingsmead Service B.V. NL-AR-000002066

Other devices from Wuhan HealthCare Biotechnology Co., Ltd.

See all devices from Wuhan HealthCare Biotechnology Co., Ltd. →

Properties

  • 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