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Urin-Monovette® 3, 2ml

by SARSTEDT AG & Co.KG FDA registration: Germany EUDAMED

Ref 10.250.002 EMDN W05010202

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number4038917SARTD00400U5K Basic UDI-DIDate28 Aug 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  • Withdrawn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 · synced 24 Oct 2026

Device Name
Urin-Monovette® Unsteril
Model / Reference
10.250.002
Primary DI / UDI-DI
04066916018467
Basic UDI-DI
4038917SARTD00400U5K
Unit of Use DI
04066916018450
EMDN Code
W05010202 Urine collection, tubes
Device Class
Class A
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005649

Other devices from Sarstedt AG & Co. KG

See all devices from Sarstedt AG & Co. KG →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 04066916018467|4038917SARTD00400U5K 61 fields · synced 24 Oct 2026