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Monidrop

by Monidor Oy Finland EUDAMED

Ref E001152, E001153Model Monidrop

EMDN V0399

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06430066950010 Basic UDI-DIDate26 Sep 2023RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Withdrawn
  • Not covered

European Union — CE/MDD Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Monidrop Infusion monitor
Model / Reference
Monidrop, E001152, E001153
Primary DI / UDI-DI
06430066950010
Basic UDI-DI
B-06430066950010
EMDN Code
V0399 Measurement devices - other
Device Class
Class I
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000007941

Other devices from Monidor Oy

  • Monidor Vitals

    Class IIb

  • IV Screen

    Class IIa

  • Monidrop W

    Class I

Properties & raw data

Show properties, registry sources and raw records
  • Measuring Function
Other properties (10)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED a849da76-ffd9-42e7-8ff7-f2793aac0f90 61 fields · synced 24 Oct 2026