Skip to content

Viofor JPS System Family +

by Med & Life Sp. z o.o. EUDAMED

Active European Union

Ref REF 1037Model Viofor JSP System

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number590515520VioforSystemRZ Basic UDI-DIDate15 Jun 2023RegisteredStatusActive
European UnionCE/MDR Number590515520VioforSystemRZ Basic UDI-DIDate15 Jun 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Viofor JSP System
Model / Reference
Viofor JSP System, REF 1037
Primary DI / UDI-DI
05905155200044
Basic UDI-DI
590515520VioforSystemRZ, B-05905155200044
Direct Marketing DI
05905155200044
EMDN Code
Z120606 Magnetotherapy equipment
Device Class
Class IIa
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000024639

Other devices from Med & Life Sp. z o.o.

See all devices from Med & Life Sp. z o.o. →

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