Device Recall EXCITE

  • Modelo / Serial
    00000249264MR3, 00000257756MR7, 00000255196MR8, 00000246630MR8, 00000259107MR1, 00000248178MR6, 00000257451MR5, 00000256200MR7, 00000260871MR9, 00000252451MR0, 00000259108MR9, 00000254480MR7, 00000254482MR3, 00000256198MR3, 00000249263MR5, 00000250755MR6, 00000251090MR7, 00000GE0131001, 00000GE0213040, 00000254375MR9, 00000GE0205028, 00000GE0210034, 00000227995MR8, 00000GE0212037, 00000GE0226049, 00000GE0410083, 00000260871MR9, 00000GE0234057, 00000GE0123041, 00000GE0302068
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide, including USA, China, Finland, Germany, Israel, Italy, Korea, Spain, and Taiwan.
  • Descripción del producto
    GE Healthcare-Americas Signa 3.0T EXCITE Whole Body Magnetic Resonance System
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    GE Medical Systems LLC, 3200 N Grandview Blvd, Waukesha WI 53188-1693
  • Source
    USFDA