Device Recall VisiPro" Biliary Stent System

  • Modèle / numéro de série
    Lot Numbers: 4089374, 4140341, 4151887, 4194358, 4239470, 4251836, 4484043, 44804047, 4491290, 4933989, 5005731, 5012045, 5045725, 5117532, 5147416, 5149205, 5214432, 5221941, 5239429, and 5577902.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution including states of AL,AZ, CA, CO, CT, FL, IL, IN, IA, KS, KY, LA,ME, MA, MI, MN, MO, MT, NJ, NY, NC, OH, OR, PA, RI, SC, TN, TX, WV, WI, and VA. Counties of SWEDEN, TUNISIA, SWITZERLAND, GERMANY, ITALY, SLOVENIA, FRANCE, BELGIUM, UNITED KINGDOM, TURKEY, FINLAND, LITHUANIA, and NORWAY.
  • Description du dispositif
    ev3" sterile EO, single Use, Visi-Pro Balloon-Expandable Biliary Stent System. || Model Numbers: PXB35-06-27-135, PXB35-06-37-080, PXB35-07-37-080, PXB35-08-17-080 , PXB35-08-27-135 , PXB35-08-37-135, PXB35-08-57-080, and PXB35-09-17-135 4800. The Endovascular Company, Nathan Lane North, Plymouth, MN 55442-2920,
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Ev3, Inc, 4600 Nathan Ln N, Plymouth MN 55442-2890
  • Source
    USFDA