Device Recall NC Stormer Zipper MX Balloon Dilation Catheter

  • Modelo / Serial
    1) PMA # P790017/S79 2) Device Listing Number 2112641 3) Facility Registration number 2953200 4) lot codes 44DOE015, 44DOE016, 44DOE019, 44DOE022, 44DOE023, 44DOE020, 44DOE024, 44DOE025, 44DOE026, 44DOE021, 44DOE029, 44DOE032 5) Item numbers NCS2506ZP, NCS3016ZP, NCS2511ZP, NCS3516ZP, NCS3511ZP, NCS3521ZP, NCS3006ZP, NCS3011ZP, NCS2516ZP, NCS4006ZP, NCS4011ZP, NCS3021ZP
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Product was distributed to 40 hospitals
  • Descripción del producto
    Percutaneous Transluminal Coronary Angioplasty system in sterile pouch.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Medtronic Vascular, 3576 Unocal Pl, Santa Rosa CA 95403-1774
  • Source
    USFDA