Device Recall Aortic Arterial Cannula 22 Fr

  • Modèle / numéro de série
    UDI CODE: 04037691123813, Lot Number: 92181729 and 92181287
  • 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 22 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002246, Article Number A22-7107. 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