Ultra 8 IAB

  • Model / Serial
    Lot Numbers: KF0087855 KF0087856 KF0098040 KF0108374 MF0011189 MF0021654 MF0032271 MF0042406 MF0042501 MF0042786 MF0053023 MF0063353 MF0073903 MF0074071 MF7065606 MF7086741 MF7118151 MF7128507 MF8103280 MF8103571 MF8113919 MF8113951 MF8124345 MF9014575 MF9014817 MF9024965 MF9024993 MF9025112 MF9025209 MF9035509 MF9035685 MF9035955 MF9046057 MF9046247 MF9046501 MF9056746 MF9057069 MF9057070 MF9067275 MF9067738 MF9067740 MF9077954 MF9078048 MF9078052 MF9078348 MF9078349 MF9088685 MF9100025 MS0053114 MS9056684 MS9056857 MS9057154 MS9110263 MS9110269
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution -- USA, Canada, Australia, Belgium, Czechoslovakia, Germany, Russia, Spain, Finland, France, Great Britain, Hungary, Italy, Netherlands, Poland, Saudi Arabia, Switzerland, Brazil, Australia, Chile, Colombia, Ecuador, India, Indonesia, Japan, Korea, Malaysia, Mexico, New Zealand, Panama, Peru, Philippines, Taiwan, Thailand, and Venezuela.
  • Product Description
    Arrow Ultra 8 IAB (Intra-Aortic Balloon) Catheter, 8 Fr, 40cc. || Model: IAB-05840-U
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Arrow International, Inc., Division of Teleflex Medical Inc., 9 Plymouth St, Everett MA 02149-1814
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

11 devices with a similar name

Learn more about the data here

  • Model / Serial
  • Product Classification
  • Product Description
    Arrow International: FiberOptix Ultra 8 IAB@ 8Fr 30cc,Ultra IAB: 8Fr 30cc, FiberOptix Ultra 8 IAB@ 8Fr 40cc, Ultra IAB: 8Fr 40cc, Ultra Flex IAB: 7.5Fr 30cc, Ultra Flex IAB: 7.5Fr 35cc, Ultra Flex IAB: 7.5Fr 40cc, RediGuard IAB: 7Fr 30cc
  • Manufacturer
  • Model / Serial
    IAB-05830-U, IAB-05840-U | See FSN
  • Product Description
    MD: Intra-aortic balloon catheter; Oximeter catheter, single-use
  • Manufacturer
6 more