Skip to content

Transport medium

by Miraclean Technology Co., Ltd 12 variants

Ref IV-Group B streptococcus transport mediumModel I-Cary Blair transport medium; II-Amies transport medium; III-Stuart transport medium; IV-Group B streptococcus transport medium.

Active European Union

CE IVDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697189332TM5U Basic UDI-DI 06971893324877UDI-DIDate22 Sep 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / Reference
I-Cary Blair transport medium, II-Amies transport medium, III-Stuart transport medium, IV-Group B streptococcus transport medium., IV-Group B streptococcus transport medium
Primary DI / UDI-DI
06971893324877
Basic UDI-DI
697189332TM5U
Direct Marketing DI
06971893324877
EMDN Code
W05020199 Samples transport, containers - other
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000011683
Authorised representative
Share info GmbH DE-AR-000005132

Other devices from Miraclean Technology Co., Ltd.

See all devices from Miraclean Technology Co., Ltd. →

Properties

  • Professional Testing

Other properties (10)

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