Device Recall Precision Link Software

  • Modèle / numéro de série
    Part Numbers: 99040-01,99063-02.99514-01,97444-04, 97444-05,97445-05,97570-04,  98891-04,98929-05,98931-04, 98889-06, 98890-05, 98891-05,  98929-06,98931-05,99063-04,  99516-03, 80378-01,80379-01,80380-01,  80381-01, 80382-01,80383-01,  80392-01, 70519-01, 80392-02
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution: USA as well as abroad to Argentina, Aruba, Australia, Austria, Bahamas, Belgium, Canada, Colombia, Croatia, Curacao, Czech/Slovak Republics, Dominican Republic, Ecuador, El Salvador, Finland, France, Germany, Greece, Guatemala, Hong Kong, Ireland, Italy, Japan, Korea, Latvia, Lithuania/Estonia (Baltics), Mexico, Netherlands, New Zealand, Norway, Poland, Puerto Rico, Portugal, Saudi Arabia, Serbia, Bulgaria/Macedonia, Singapore, Slovenia, South Africa, Spain, St. Maarten, Sweden, Switzerland, Turkey, UK and Venezuela.
  • Description du dispositif
    Abbott Precision Link Software (Version 2.1), (Version 2.2), (Version 2.3), (Version 2.4), (Version 2.5), and (Version 2.6); Serial Number(s): ALL;
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Abbott Diabetes Care, Inc., 1360 S Loop Rd, Alameda CA 94502-7000
  • Source
    USFDA