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Pregnancy Associated Plasma Protein-A Chemiluminescent Immunoassay Kit

by Maccura Biotechnology Co., Ltd. 2 variants

Ref IM4493073, IM4402073, IM4406073, IM4407073, IM4494073

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 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-IM4493073M3 Basic UDI-DI Date22 May 2022RegisteredStatusActive

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  • Withdrawn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
Pregnancy Associated Plasma Protein-A Chemiluminescent Immunoassay Kit
Model / Reference
IM4493073, IM4402073, IM4406073, IM4407073, IM4494073
Primary DI / UDI-DI
D-IM4493073M3, D-IM4402073HR, D-IM4406073JM, D-IM4407073JU, D-IM4494073MA
Basic UDI-DI
B-IM4493073M3, B-IM4402073HR, B-IM4406073JM, B-IM4407073JU, B-IM4494073MA
EMDN Code
W0102050210 Pregnancy associated plasma protein - a (downs)
Device Class
Class IVD General
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
CN-MF-000014618
Authorised representative
Humiss International B.V. NL-AR-000001490

Other devices from Maccura Biotechnology Co., Ltd.

See all devices from Maccura Biotechnology Co., Ltd. →

Properties

  • Human Tissues
  • Animal Tissues
  • Reagent
  • Professional Testing

Other properties (6)

  • Sterile: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No