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Watin Biolife

by Watin Biolife Manufacturing Company Saudi Arabia EUDAMED

Ref 1133

EMDN W0104010206

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number628704495032MIOW3 Basic UDI-DIDate6 May 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
M.I.O. (Motility Indole Ornithine) Medium
Model / Reference
1133
Primary DI / UDI-DI
06287044950322
Basic UDI-DI
628704495032MIOW3
EMDN Code
W0104010206 Media in tubes (solid & liquid)
Device Class
Class A

Manufacturer details

EUDAMED SRN
SA-MF-000047358
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Watin Biolife Manufacturing Company

See all devices from Watin Biolife Manufacturing Company →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 903a5470-ca5f-4d3e-b7af-9530e2258530 61 fields · synced 22 Oct 2026