ArjoHuntleigh AB

3 dispositivos en la base de datos

  • Modelo / Serial
    Model Number: GAB1000-01 and GAB1000-11 Serial Number: From 810000957 up to T3387
  • Descripción del producto
    Medical devices in hospital equipment
  • Modelo / Serial
    Model Number: 526000-03, 526000-04, 526000-07, 526000-08, 526000-09, 526000-10 Serial Number: Devices with software V1.099 manufactured from Sep 26, 2014 through Dec 20, 2016 Range of affected serial numbers: 1400028031 to 1600048470
  • Descripción del producto
    Electromechanical medical devices
  • Modelo / Serial
    Model Number: BAB1000-01 / BAB5000-01 Serial Number: P0230959 P0311257 P0233762 P0315544 P0235631 P0315545 P0285193 P0315546 P0285194 P0315547 P0285191 P0315548 P0288108 P0315549 P0288358 P0315550 P0288359 P0315551 P0288360 P0315552 P0288361 P0315553 P0291845 P0315787 P0296662 P0315788 P0297220 P0315789 P0298334 P0315790 P0300851 P0315791 P0301373 P0315792 P0301374 P0315793 P0311256 P0315794
  • Descripción del producto
    Medical devices for the disabled

16 fabricantes con un nombre similar

Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Source
    NZMMDSA
  • Empresa matriz del fabricante (2017)
  • Source
    MSHM
  • Empresa matriz del fabricante (2017)
  • Source
    AEMPSVFOI
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    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
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