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Mueller Hinton Ii Agar

by Sundial Co. Ltd EUDAMED

Active European Union

Ref SUN12130, SUN90130

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number5298004040541YE Basic UDI-DIDate30 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
SUN12130, SUN90130
Primary DI / UDI-DI
05298004040541, 05298004040015
Basic UDI-DI
5298004040541YE, 5298004040015XL
EMDN Code
W0104010403 Susceptibility test media (plates)
Device Class
Class A
Market of Registration
Cyprus

Manufacturer details

EUDAMED SRN
CY-MF-000023765

Other devices from Sundial Co. Ltd

See all devices from Sundial Co. Ltd →

Properties

  • Sterile
  • Reagent
  • Professional Testing

Other properties (8)

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