Devices

Device Recall RS 5F DL XPP

  • Modelo / Serial
    UPN: H96560M0303931; Lot: 5304317, 5304317
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    The products were distributed to the following US states: AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, WA, WI, and WV. The products were distributed to the following foreign countries: Canada, China, Ireland, Spain.
  • Descripción del producto
    RS 5F DL XPP, Catalog Number 60M030393
  • Manufacturer
    Angiodynamics Inc. (Navilyst Medical Inc.)
  • 1 Event

Fabricante

Angiodynamics Inc. (Navilyst Medical Inc.)
  • Dirección del fabricante
    Angiodynamics Inc. (Navilyst Medical Inc.), 10 Glens Falls Tech Park, Glens Falls NY 12801-3864
  • Empresa matriz del fabricante (2017)
    AngioDynamics Inc
  • Source
    USFDA

Dispositivo con un nombre similar

Más información acerca de la data acá

Device Recall RS 5F DL XPP KIT
  • Modelo / Serial
    UPN: H96560M1831041; Lot: 5310755
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    The products were distributed to the following US states: AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, WA, WI, and WV. The products were distributed to the following foreign countries: Canada, China, Ireland, Spain.
  • Descripción del producto
    RS 5F DL XPP KIT, Catalog Number 60M183104
  • Manufacturer
    Angiodynamics Inc. (Navilyst Medical Inc.)