ArjoHuntleigh AB

9 devices in the database

  • Model / Serial
    Model: Models: 380 & 480, Affected: Manufactured between 12 January 2011 to 31 December 2011
  • Model / Serial
    Model: Models: 1000 & 1080, Affected: All serial numbers
  • Model / Serial
    Model: Tenor without scale, Affected: All devices manufactured since 2004
  • Model / Serial
    Model: A5962, Affected:
  • 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