Devices

Device Recall MultiDiagnost MD4

  • Modèle / numéro de série
    Site Numbers: 6842, 10388, 10458, 13172, 13258, 13704, 13721, 13879, 13918, 35484, 38501, 38635, 38783, 38912, 38917, 38929, 38944, 41000, 41031, 41069, 41111, 41143, 41439, 44898, 45039, 45042, 50251, 50328, 50340, 52455, 52471, 62938, 76804, 76808, 76834, 76975, 82628, 82687, 83038, 83367, 83957, 84463, 84892, 84930, 85034, 85491, 85694, 86218, 86328, 87030, 87140, 87176, 87302, 100700, 100954, 101038, 101153, 101156, 101759, 101863, 102034, 102562, 102583, 103023, 103209, 103210, 103377, 103651, 103855, 104137, 104589, 105022, 536135, 557747, 557867, 557972, 557998, 558099, 558203, 558270, 49794053 (or 6838), and 49788736 (or 6842).
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution
  • Description du dispositif
    MultiDiagnost MD4
  • Manufacturer
    Philips Medical Systems North America Co. Phillips
  • 1 Event

Fabricant

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