Philips Medical Systems Nederland BV

5 devices in the database

  • Model / Serial
    Model Number: 722026; 722027; 722028; 722029; 722033; 722034; 722035; 722038; 722039; 722058; 722059 with release R8.2 (Allura Xper) or R1.0 (UNIQ)
  • Product Description
    Medical devices for diagnostics and radiation therapy
  • Model / Serial
    Model Number: 708032, 708033, 708034, 708036, 708037, 708038
  • Product Description
    Medical devices for diagnostics and radiation therapy
  • Model / Serial
    Model Number: 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722015, 722019, 722020, 722022, 722023, 722025, 722026, 722027, 722028, 722029, 722031, 722033, 722034, 722035, 722038, 722039, 722058 and 722400.
  • Product Description
    Medical devices for diagnostics and radiation therapy
  • Model / Serial
    Model Number: 722010, 722011, 722012, 722013, 722022, 722023, 722024, 722025
  • Product Description
    Medical devices for diagnostics and radiation therapy
  • Model / Serial
    Catalog Number: See UAL Model Number: 722010, 722011, 722012, 722013, 722022, 722023, 722024, 722025 and all other eventual model numbers mentioned on the Unit Affected List.
  • Product Description
    Medical devices for diagnostics and radiation therapy

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