Device Recall GE Healthcare RFX

  • Modèle / numéro de série
    Mfg. Lot or Serial # System ID Not Available 818963RM4 00000026176YY8 213266SFX Not Available 209384MMRF 00000047956YY8 INSIGHTXR010 Not Available 818891VA1 Not Available 818891VA2 Not Available 2025761X46 Not Available 2025761X40 Not Available 813633RFX Not Available 813971RF6 Not Available 708259NWRF7 00000034249YY3 913596PR4 00000023702YY4 606327ADV Not Available 504867LRF2 Not Available 318388RF3 00000023806YY3 617735B6 00000022210YY9 313576RM1663 00000022218YY2 313576RM3622 Not Available 313576RM3645 Not Available 218726SMRF2 Not Available 601865RF1 Not Available 601865RF2 Not Available 601376OP3 Not Available 919681DB3 Not Available 919250WM9 00000026194YY1 706791D7 Not Available 914964SJRF 00000071239YY8 405271PRF4 00000022200YY0 215576RF18 00000128622MO8 615871SRF1 Not Available 817965HADV Not Available 713364W03 Not Available 206244RM2 00000022207YY5 EG1055VA01 00000022140YY8 SK1005RX05 00000023856YY8 AE1020RX01
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    US: AL, AR, AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT,NC, NE NH, NJ, NM, NY, NV, OH, OK, PA, RI, SC, SD, TN, TX,, VA, WA, WO, WY, WV. OUS: Algeria Armenia Australia Austria Brazil Canada Chile China Denmark Egypt France Germany Guatemala Honduras Hong Kong Hungary Iceland India Ireland Italy Japan Korea Libya Mexico Netherlands Netherlands Peru Poland Portugal Russia Saudi Arabia Serbia Sierra Leone Slovakia Spain Taiwan Thailand Turkey United Arab Emirates United Kingdom Venezuela Vietnam
  • Description du dispositif
    RFX
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    GE Healthcare, LLC, 3000 N Grandview Blvd, Waukesha WI 53188-1615
  • Société-mère du fabricant (2017)
  • Source
    USFDA