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Docteur B

by Hubei MEIBAO Biotechnology Co., Ltd 6 variants

Ref HCG-M35D02(2 Tests/Kit)Model Midstream

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 linked in EUDAMED

A group certificate may exist

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-26957290300168 Basic UDI-DI Date5 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Active

Specification

EUDAMED

Device Name
One Step HCG Pregnancy Test
Model / Reference
Midstream, HCG-M35D02(2 Tests/Kit)
Primary DI / UDI-DI
26957290300168, 26957290300151
Basic UDI-DI
B-26957290300168, B-26957290300151
EMDN Code
W0102160302 Hcg - rt & poc
Device Class
Class IVD devices for self-testing
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000019986
Authorised representative
Sungo Cert GmbH DE-AR-000010869

Other devices from Hubei MEIBAO Biotechnology Co., Ltd

See all devices from Hubei MEIBAO Biotechnology Co., Ltd →

Properties

  • Reagent
  • Self Testing

Other properties (8)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No