Philips Medical Systems Nederland BV

9 devices in the database

  • Model / Serial
    881001
  • Product Description
    MD: Full-body CT system
  • Model / Serial
    722026, 722027, 722028, 722029, 722033, 722034, 722035, 722038, 722039, 722058, 722059 | R8.2
  • Product Description
    MD: Stationary general-purpose fluoroscopic x-ray system, analogue
  • Model / Serial
    722026, 722027, 722028, 722029, 722033, 722034, 722035, 722038, 722039, 722058, 722059 | R 1.0
  • Product Description
    MD: Stationary general-purpose fluoroscopic x-ray system, analogue
  • Model / Serial
    708032, 708033, 708034, 708036, 708037, 708038 | several
  • Product Description
    MD: Stationary general-purpose fluoroscopic x-ray system, analogue
  • Model / Serial
    881005 | see FSN | IntelliSpace Portal V.6.5
  • Product Description
    MD: Food tray, single-use
4 more

12 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
  • 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
7 more