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Activ 701

by Indiba S.A.U. EUDAMED

Withdrawn No longer placed on the EU market

Ref ACT207

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8434251D2Z00000000BT Basic UDI-DIDate18 Mar 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Radiofrequency Devices Os
Model / Reference
ACT207
Primary DI / UDI-DI
08434251000601
Basic UDI-DI
8434251D2Z00000000BT
EMDN Code
Z120602 Physiotherapy equipment
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
ES-MF-000001243

Other devices from Indiba S.A.U.

See all devices from Indiba S.A.U. →

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