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Blood Enrichment Culture Bottles

by Taho Future ( Tianjin ) Biotechnology Co., Ltd EUDAMED

Active European Union

Ref TB-25

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697650495BCS11K5 Basic UDI-DIDate23 Oct 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDR Active

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

Specification

EUDAMED

Model / Reference
TB-25
Primary DI / UDI-DI
16976504953191, 06976504952319
Basic UDI-DI
697650495BCS11K5
EMDN Code
W0104010604 Manual mycobacteria media (tubes & bottles)
Device Class
Class A
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000037788
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from Taho Future ( Tianjin ) Biotechnology Co., Ltd

See all devices from Taho Future ( Tianjin ) Biotechnology Co., Ltd →

Properties

  • Animal Tissues
  • Reagent
  • Professional Testing

Other properties (8)

  • Sterile: No
  • Human Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No