Product is a Powerflex P3 Dialation Catheter. Product is labeled in part: ''***POWERFLEX P3***Cordis***a Johnson and Johnson company***ENDOVASCULAR***STERILE EO***Cordis Europa N.V., 9301 LJ Roden, The Netherlands***''

Fabricante

  • Dirección del fabricante
    Cordis Corporation, 14201 NW 60th Ave, Miami Lakes FL 33014-2802
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA