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ARC-EX System Professional

by Onward Medical N.V. Netherlands EUDAMED

Ref EXSYS01PROEU5

EMDN N010103

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number872090831000EXSYS01TP Basic UDI-DIDate8 Sep 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
ARCEX System
Model / Reference
EXSYS01PROEU5
Primary DI / UDI-DI
08720908310095
Basic UDI-DI
872090831000EXSYS01TP
EMDN Code
N010103 Bipolar nervous electrostimulators, battery-powered
Device Class
Class IIa
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
NL-MF-000022388

Other devices from Onward Medical N.V.

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 1fe786de-6764-49a0-87c8-87dc0a198a68 61 fields · synced 23 Oct 2026