Device Recall Diagnost 56/66/76/76 Plus

  • Modèle / numéro de série
    Devices are identified as Site Numbers:  73421, 46653, 59224, 62325, 13479, 46954, 25563, 61812, 34800, 13612, 13624, 68220, 35590, 68219, 17576, 59474, 35420, 62630, 44890, 41239, 13691, 59011, 47149, 44888, 6709, 6824, X1007, and X1775.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    Diagnost 56/66/76/76 Plus, DSI is a Spot-Film and has a Digital Imaging Spot. || Intended use is for the following applications: as a multifunctional/universal system, general R/F, Fluoroscopy, Radiology, and Angiography can be performed along with pediatric examinations and more specialized interventional applications.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Philips Medical Systems North America Co. Phillips, 22100 Bothell Everett Hwy, Bothell WA 98021-8431
  • Source
    USFDA