Skip to content

Mediu Mannitol Motilitate Test

by Deltarom SRL EUDAMED

Active European Union

Ref 343625, 343627, 3436225

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number594054038MEDIUMANNITOLMLV Basic UDI-DIDate9 Jul 2025RegisteredStatusActive

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  • Withdrawn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
343625, 343627, 3436225
Primary DI / UDI-DI
05940540386064, 05940540386033, 05940540386057
Basic UDI-DI
594054038MEDIUMANNITOLMLV, 594054038MEDIUMANNITOL2K9, 594054038MEDIUMANNITOL0K5
EMDN Code
W0104010101, W0104010206, W0104010306
Device Class
Class A
Market of Registration
Romania

Manufacturer details

EUDAMED SRN
RO-MF-000035924

Other devices from Deltarom SRL

See all devices from Deltarom SRL →

Properties

  • Reagent
  • Professional Testing

Other properties (9)

  • Sterile: No
  • 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