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NeuroTrac® MyoPlus Pro XE

by Verity Medical Ltd. EUDAMED

Active European Union

Ref MYO120PX

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506007397MYO120PXPX Basic UDI-DIDate9 Sep 2026RegisteredStatusActive

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  • Withdrawn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 system with EMG of physiotherapy, a rechargeable battery
Model / Reference
MYO120PX
Primary DI / UDI-DI
05060073970445
Basic UDI-DI
506007397MYO120PXPX
EMDN Code
Z12062899 Neuromuscular stimulation equipment - other
Device Class
Class IIa
Market of Registration
Norway

Manufacturer details

EUDAMED SRN
IE-MF-000007426

From the manufacturer

Manufacturer's product page: View Product

Other devices from Verity Medical Ltd.

See all devices from Verity Medical Ltd. →

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