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Mai Device

by Neurostimulation Medtech Private Limited EUDAMED

Active European Union

Ref MA0222Model Variant: First Relief

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8908006064MA0222WQ Basic UDI-DIDate20 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2026-MDR/QS-044 Issued

    Quality management system EU MDR

    Notified body
    3EC International a.s. 2265
    Issued
    1 Jul 2026
    Expires
    1 Jul 2031

Specification

EUDAMED

Device Name
NeuroStimulation Device – MAI DEVICE
Model / Reference
Variant: First Relief, MA0222
Primary DI / UDI-DI
08908006064410
Basic UDI-DI
8908006064MA0222WQ
EMDN Code
Z120623 Acupuncture stimulators
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IN-MF-000048305
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Neurostimulation Medtech Private Limited

See all devices from Neurostimulation Medtech Private Limited →

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