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Vmk Endoneedle

by Nipro Corporation EUDAMED

Active European Union

Ref EN-2825-ETModel VMK ENDONEEDLE

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05420040815399 Basic UDI-DIDate6 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Rinsing root canal
Model / Reference
VMK ENDONEEDLE, EN-2825-ET
Primary DI / UDI-DI
05420040815399
Basic UDI-DI
B-05420040815399
EMDN Code
A010602 Dental irrigation needles
Device Class
Class I
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
JP-MF-000026759
Authorised representative
Nipro Medical Europe NV BE-AR-000022416

Other devices from Nipro Company, Ltd.

See all devices from Nipro Company, Ltd. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No