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Linova-X Electrotherapy Stimulator

by Linova-X Tech Co., Ltd. EUDAMED

Active European Union

Ref PM002

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number698052041EMS01CD Basic UDI-DIDate24 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Linova-X Electrotherapy Stimulator
Model / Reference
PM002
Primary DI / UDI-DI
06980520410029
Basic UDI-DI
698052041EMS01CD
Direct Marketing DI
06980520410029
EMDN Code
Z12062801 Muscle reinforcement stimulators for innervated muscles
Device Class
Class IIa
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000058730
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Linova-X Tech Co., Ltd.

See all devices from Linova-X Tech Co., 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