BeGraft Peripheral Plus Stent Graft System

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ

6 devices with a similar name

Learn more about the data here

  • Model / Serial
  • Implanted device?
    Yes
  • Product Description
    Non-active implants - special implants
  • Manufacturer
  • Model / Serial
  • Implanted device?
    Yes
  • Product Description
    Implant
  • Manufacturer
  • Model / Serial
  • Product Description
    Bentley InnoMed: BeGraft Peripheral Plus Stent Graft System
  • Manufacturer
  • Model / Serial
    BGP+2707_2BGP+3707_2BGP+5707_2BGP+2708_2BGP+3708_2BGP+5708_2 | All LOT numbers of the above mentioned catalogue numbers
  • Product Description
    MD: Stent Graft System
  • Manufacturer
One more