Device Recall Guidant

Manufacturer

  • Manufacturer Address
    Guidant Corp-Cpi Division, 4100 N Hamline Ave, St Paul MN 55112-5798
  • Source
    USFDA

45 devices with a similar name

Learn more about the data here

  • Model / Serial
    All Serial numbers
  • Product Classification
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    Nationwide in the United States and worldwide.
  • Product Description
    Contak TR Multiprogrammable Pacemaker, DDDR Model 1241
  • Manufacturer
  • Model / Serial
    Serial numbers 110685, 110687, 110688, 110706, 110708, 110709, 110710, 110711, 110712, 110713 110714, and 110715
  • Product Classification
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    Nationwide in the United States and worldwide.
  • Product Description
    Pulsar Max II Multiprogrammable Pacemaker, Model 1180
  • Manufacturer
  • Model / Serial
    Serial number 811798
  • Product Classification
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    Nationwide in the United States and worldwide.
  • Product Description
    Pulsar Max II Multiprogrammable Pacemaker, Model 1181
  • Manufacturer
  • Model / Serial
    Serial numbers 206555, 206557, 206558, 206559, 206560, 206561, 206562, 206525, 206526, 206527, 206528, and 206529
  • Product Classification
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    Nationwide in the United States and worldwide.
  • Product Description
    Discovery II Multiprogrammable Pacemaker, Model 0981
  • Manufacturer
  • Model / Serial
    Serial numbers 319492, 319493, 319494, 319495, 319496, 319497, 319498, 319499, 319500, 319501, 319502, 319503, 319505, 319506, and 319507
  • Product Classification
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    Nationwide in the United States and worldwide.
  • Product Description
    Discovery II Multiprogrammable Pacemaker, Model 1184
  • Manufacturer
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