Devices

Device Recall OmniDiagnost

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

Un dispositif médical avec un nom similaire

En savoir plus sur les données ici

Device Recall OmniDiagnost
  • Modèle / numéro de série
    OmniDiagnost User Interface PN 9896 000 59561, 9896 000 12381, 9896 000 58161;  The firm utilizes a ''site number'' specific to each unit: 101599, 103055, 103058, 100520, 100873, 101152, 101154, 101676, 101962, 102164, 102582, 102977, 103050, 103051, 103052, 103055, 103058, 103218, 103219, 104012, 104577, 104858, 104934, 105324, 105394, 13124, 38351, 50428, 76596, 76944, 76948, 82655, 83871, 83958, 84441, 84850, 85163, 85165, 86113, 86303, 86326, 86339, 86340, 86485, 86486, 86549, 86965, 86977, 87164, X1707, X1747, 104857
  • Classification du dispositif
    Radiology Devices
  • Distribution
    The firm distributed devices to 81 hospitals and medical centers located throughout the U.S.
  • Description du dispositif
    OmniDiagnost System
  • Manufacturer
    Philips Medical Systems Sales & Service Region No. America