Device Recall Philips MultiDiagnost Eleva with Digital Image (DI) Rel.2 system

  • Modèle / numéro de série
    Site Numbers:   105193, 505346, 506247, 520046, 532151, 532213, 534247, 535714, 535767, 536019, 536091, 536146, 536720, 536935, 537083, 537669, 537787, 539457, 539598, 539990, 540252, 541263, 541474, 543272, 544059, 545014, 545156, 545198, 545841, 546031, 546578, 549417, 551519, 553138, 553139, 553140, 553287, 554015, 554687, 554689, 554730, 556197, and 42381879.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide distribution: USA including states of: AZ, CA, CO, CT, DE, FL, GA, HI, ID, LA, MA, ME, MI, MN, MO, MS, NC, NJ, NV, NY, OH, OR, PA, SC, TN, TX, VA, WA, WI, and WY.
  • Description du dispositif
    Philips MultiDiagnost Eleva with Digital Image (DI) Rel.2 system. || The Philips MultiDiagnost Eleva is intended use as a multi-functional universal system, general RF, Fluoroscopy, Radiography and Angiography can be performed along with more specialized interventional applications.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Philips Medical Systems North America Co. Phillips, 22100 Bothell Everett Hwy, Bothell WA 98021-8431
  • Source
    USFDA