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Kinetec Centura B&W

by Kinetec SAS France EUDAMED

Ref 462100360X, 4621003102Model Centura EMDN Z120603

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376024624SHOULDERCPMCG Basic UDI-DIDate18 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Trade Name
Kinetec Centura B&W
Centura
Model / Reference
Centura, 462100360X, 4621003102
Primary DI / UDI-DI
03760246246927, 03760246246903
Basic UDI-DI
376024624SHOULDERCPMCG
EMDN Code
Z120603 Passive rehabilitative gymnastics equipment
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000364

Other devices from Kinetec SAS

See all devices from Kinetec SAS →

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 (2)

  • EUDAMED 6caa49ae-20ee-4416-b225-886493bd2515 61 fields · synced 22 Oct 2026
  • EUDAMED 03760246246903|376024624SHOULDERCPMCG 61 fields · synced 18 May 2026