Philips Medical Systems Nederland BV

9 dispositifs dans la base de données

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

12 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Société-mère du fabricant (2017)
  • Source
    NZMMDSA
  • Société-mère du fabricant (2017)
  • Source
    AEMPSVFOI
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    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
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    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 en plus