ArjoHuntleigh AB

8 devices in the database

  • Model / Serial
    700-19490, 700-19485 | 700-19490: starting from serial number 300142013 up to serial number 300219867, 700-19485: starting from serial number 300146551 up to serial number 300220716
  • Product Description
    MD: Mobile patient lifting system, battery-powered
  • Model / Serial
    526000-03, 526000-04, 526000-07, 526000-08, 526000-09, 526000-10;n/a | / | Devices with software V1.099 manufactured from Sep 26, 2014 through Dec 20, 2016 Range of affected serial numbers: 1400028031 to 1600048470 | 1.099
  • Product Description
    MD: Intermittent venous compression system
  • Model / Serial
    APA1000-XX | P0298176, P0323011, P0361422, P0361423, P0363456
  • Product Description
    MD: Mobile patient lifting system, battery-powered
  • Model / Serial
    devices manufactured between 7th March 2014 and 20th April 2015 | P0227712, P0227711,P0233765
  • Product Description
    MD: Bathing table, portable
  • Model / Serial
    8259965-R | M9-97-001, 30576839, M9-97-002, 60470085, 100473367
  • Product Description
    MD: Kinetic bed
3 more

16 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Parent Company (2017)
  • Source
    NZMMDSA
  • 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
11 more