ArjoHuntleigh AB

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Description

9 devices in the database

  • Model / Serial
    Model: , Affected: Serial numbers within a range between P0167499 and P0418644
  • Model / Serial
    Model: , Affected: Serial number range from 1600031138 up to 1700046457
  • Model / Serial
    Model: , Affected: Software V1.099, Serial Numbers range from 1400028031 to 1600048470
  • Model / Serial
    Model: Maxi Move Units, Affected: 300043863 to 300100386
  • Model / Serial
    Model: , Affected: batch of devices manufactured between 7th March 2014 and 20th April 2015.
4 more

16 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Parent Company (2017)
  • Source
    AEMPSVFOI
  • 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
  • Manufacturer Parent Company (2017)
  • Source
    AMPMDRS
11 more