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IL-2RA/IL-18/IL-33/IL-23/IL-27/IL-22 detection kit (Flow cytometry)

by Qingdao Raisecare Biological Technology Co., Ltd. 3 variants

Ref 50 tests

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-06972227432015 Basic UDI-DI 06972227432015UDI-DIDate7 Jun 2023RegisteredStatusActive

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  • Withdrawn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
IL-2RA/IL-18/IL-33/IL-23/IL-27/IL-22 detection kit (Flow cytometry)
Model / Reference
50 tests
Primary DI / UDI-DI
06972227432015
Basic UDI-DI
B-06972227432015
EMDN Code
W0103080699 Reagents for flow cytometry - other
Device Class
Class IVD General
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
CN-MF-000033899
Authorised representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

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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