Device Recall CDI 500 Blood Parameter Monitoring System

  • Modèle / numéro de série
    1193, 1355, 1356, 1420, 1423, 1464, 1465, 1504, 1521, 1522, 1523, 1524, 1526, 1527, 1529, 1530, 1602, 1603, 1604, 1606, 1662, 2035, 2102, 2103, 2104, 2105, 2106, 2107, 2800, 2901, 2902, 3131, 3132, 3133, 3134, 3135, 3261, 3262 and 4132.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution: USA (nationwide) and countries of : Australia, Barbados, Belgium, Brazil, Columbia, Costa Rica, Dominican Republic, Ecuador, El Salvador, Guatamala, Hong Kong, Honduras, Jordan, Japan, Libya, Mexico, Malaysia, Panama, PH, Saudi Arabia, Singapore, South Africa, Thailand, Trinidad, Taiwan and Uruguay, Germany, Saudia Arabia, Paraguay, South Korea, Dominican Republic, Phillipines, South Africa and UAE.
  • Description du dispositif
    CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules, Catalog 500AV, Terumo Cardiovascular Systems || The CDI 500 is indicated for use to display patient blood gas values during extracorporeal procedures.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Terumo Cardiovascular Systems Corporation, 6200 Jackson Road, Ann Arbor MI 48103-9586
  • Société-mère du fabricant (2017)
  • Source
    USFDA