Device Recall Aortic Arterial Cannula 24 Fr

  • Modèle / numéro de série
    UDI CODE: 04037691239804, Lot Number: 92180017, 92183437 and 92184278
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution including US state of VA and Puerto Rico, Australia, Belgium, Brazil, Canada, Chile, Colombia, Cuba, Cyprus, Czech Republic, Denmark, Egypt, Estonia, Finland, France, Germany, Iran, Ireland, Israel, Italy, Japan, Lebanon, Malaysia, Martinique, Mauritius, Mexico, Netherlands, New Zealand, Norway, Pakistan, Poland, Portugal, Reunion, Russia, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Syria, Thailand, Turkey, United Arab Emirates, and United Kingdom.
  • Description du dispositif
    Aortic Arterial Cannula 24 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002267, Article Number A24-7107. For use in cardiopulmonary bypass
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Maquet Cardiopulmonary Ag, Kehler Strasse 31, Rastatt Germany
  • Société-mère du fabricant (2017)
  • Source
    USFDA