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Kinetec SAS

by Kinetec SAS France EUDAMED

Ref 46210060X3Model Kinetec Optima S4

EMDN Z120603

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376024624KNEECPMGJ Basic UDI-DIDate22 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Kinetec Optima S4
Model / Reference
Kinetec Optima S4, 46210060X3
Primary DI / UDI-DI
03760246246811
Basic UDI-DI
376024624KNEECPMGJ
Direct Marketing DI
03760246246811
EMDN Code
Z120603 Passive rehabilitative gymnastics equipment
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
FR-MF-000000364

Other devices from Kinetec SAS

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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 2ac184f6-f3e1-496b-a5b7-fb4ff116de74 61 fields · synced 24 Oct 2026