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Thayer–Martin agar, selektiivinen agarmalja

by Tammer BioLab Oy

Ref T043Model MTM+VCNT

Active European Union

CE IVDR 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberB-06430080100170 Basic UDI-DI Date12 Nov 2024RegisteredStatusActive
European UnionCE/IVDD NumberB-06430080100170 Basic UDI-DI Date12 Nov 2024RegisteredStatusActive

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  • Withdrawn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, CE/IVDD Active

Specification

EUDAMED

Model / Reference
MTM+VCNT, T043
Primary DI / UDI-DI
06430080100170, 06430080100163
Basic UDI-DI
B-06430080100170, 643008010T043XL
EMDN Code
W0104010405 Non-chromogenic media (plates)
Device Class
Class IVD General
Class A
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000010901

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Properties

  • Animal Tissues
  • Reagent NoEUDAMEDYesEUDAMED
  • Professional Testing
  • Surgical Instrument YesEUDAMEDNoEUDAMED

Other properties (7)

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