Philips Healthcare Ingenuity Core Computed Tomography Xray system

  • Modèle / numéro de série
    Model No. 728321; S/N: 52007, 52008, 52010, 52013, 52014, 52015, 52018, 52019, 52020, 52021, 52024, 52027, 52032, 52033, 52034, 52035, 52036, 52037, 52038, 52040, 52041, 52042, 52045, 52046, 52047, 52048, 52051, 52053, 52055, 52057, 52058, 52060, 52064, 52065, 52067, 52068, 52069, 52070, 52075, 52078, 310017, 310026, 310039, 310042, 310052, 310055, 310059, 310064, 310069, 310071, 310081, 310088, 310098, 310111, 310113, 310119, 310121, 310133, 310143, 310144, 310149, 310151, 310157, 310159, 310160, 310204, 310205, 310206, 310208, 310209, 310210, 310211, 310212, 310213, 310215, 310216, 310217, 310219, 310220, 310223, 310224, 310225, 310226, 310228, 310231, 333002, 333009, 333014, 333015, 333030, 333031, 333037, 333042, 333043, 333044, 333046, 333048, 333049, 333050, 333052, 333053, 333054, 333055, 333056, 333058, 333059, 333060, 333061, 333062, 333063, 333065, 333066, 333067, 333069, 333070, 333072, 333073, 333074, 333075, 333076, 333077, 333078, 333079, 333080, 333081, 333082, 333086, 333087, 333090, 333091, 333093, 333101, 333110 & 333112.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution. US nationwide, Australia, Austria, Bangladesh, Belgium, Brazil, Cambodia, Canada, China, Egypt, France, Germany, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Korea, Lebanon, Libya, Lithuania, Malaysia, Martinique, Myanmar, Mexico, Mozambique, Netherlands, New Zealand, Norway, Palestine, Panama, Philippines, Poland, Portugal, Russia, Saudi Arabia, Singapore, Slovakia, Spain, Sweden, Switzerland, Tanzania, Thailand, Tunisia, Turkey, United Arab Emirates, United Kingdom, Uzbekistan & Vietnam.
  • Description du dispositif
    Ingenuity Core Computed Tomography X-ray system
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Philips Medical Systems (Cleveland) Inc, 595 Miner Rd, Cleveland OH 44143-2131
  • Société-mère du fabricant (2017)
  • Source
    USFDA