Device Recall Multi Diagnost Eleva

  • Modèle / numéro de série
    Site numbers 103056, 104136, 521113 102666, 104083, 104530, 105193, 105194, 105394, 504340, 504341, 505039, 505345, 505346, 506155, 506236, 506247, 519574, 532087, 532140, 532151, 532213, 532703, 533312, 533473, 533559, 534247, 535714, 535767, 536019, 536091, 536146, 536720, 536935, 537083, 537669, 537787, 538440, 539457, 539598, 539990, 540252, 541263, 541474
  • 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 Multi 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