Device Recall EXCITE

  • Modèle / numéro de série
    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
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide, including USA, China, Finland, Germany, Israel, Italy, Korea, Spain, and Taiwan.
  • Description du dispositif
    GE Healthcare-Americas Signa 3.0T EXCITE Whole Body Magnetic Resonance System
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    GE Medical Systems LLC, 3200 N Grandview Blvd, Waukesha WI 53188-1693
  • Source
    USFDA