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Kegel8® Mother Nurture

by Verity Medical Ltd. EUDAMED

Active European Union

Ref OPH310

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506007397OPH3104V Basic UDI-DIDate3 May 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered
Model / Reference
OPH310
Primary DI / UDI-DI
05060073970513
Basic UDI-DI
506007397OPH3104V
Direct Marketing DI
05060073970513
EMDN Code
Z12062899 Neuromuscular stimulation equipment - other
Device Class
Class IIa
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
IE-MF-000007426

Other devices from Verity Medical Ltd.

See all devices from Verity Medical Ltd. →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • 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