Device Recall Omni Diagnost Eleva

  • Modèle / numéro de série
    Site numbers 500046, 520020, 521648, 522220, 533112, 533314, 533471, 533530, 535118, 535257, 535924, 539106, 540860, 541490
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Units were distributed to 1543 hospitals and medical centers throughout the US. No international distribution from this firm.
  • Description du dispositif
    Philips Omni Diagnost Eleva
  • Manufacturer
  • 1 Event

Fabricant

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