Device Recall Broncho Flexible Fiberscope

  • Modelo / Serial
    C1140, C1140E, C1160, C1160E, QKC1750, QKC1750E, QKC1694, QKC1694E
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution.
  • Descripción del producto
    Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. || " Examination and treatment of the tracheobronchial tree Contraindications for Bronchoscopy " Uncontrolled angina, uncontrolled heart failure, or serious uncontrolled ventricular arrhythmias " Uncontrolled hypertension " Bleeding disorder or use of anticoagulants.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Karl Storz Endoscopy America Inc, 15 Wells St, Southbridge MA 01550-4503
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA