Device Recall Broncho Flexible Fiberscope

  • Modèle / numéro de série
    C1140, C1140E, C1160, C1160E, QKC1750, QKC1750E, QKC1694, QKC1694E
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    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

Fabricant

  • Adresse du fabricant
    Karl Storz Endoscopy America Inc, 15 Wells St, Southbridge MA 01550-4503
  • Société-mère du fabricant (2017)
  • Source
    USFDA