Guidant

11 dispositivos en la base de datos

  • Modelo / Serial
  • Descripción del producto
    Injections / Infusions / Transfusions / Dialysis
  • Modelo / Serial
  • Descripción del producto
    Medical instruments for use in humans
  • Modelo / Serial
  • ¿Implante?
    Yes
  • Descripción del producto
    Active implantable medical devices
  • Modelo / Serial
  • ¿Implante?
    Yes
  • Descripción del producto
    Active implantable medical devices
  • Modelo / Serial
  • ¿Implante?
    Yes
  • Descripción del producto
    Active implantable medical devices
6 más

34 fabricantes con un nombre similar

Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    MSHM
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    MSHM
  • Source
    LAANSM
  • Dirección del fabricante
    Guidant Corp-Cpi Division, 4100 N Hamline Ave, St Paul MN 55112-5798
  • Source
    USFDA
  • Dirección del fabricante
    Guidant Corporation ACS, 26531 Ynez Road, Temecula CA 92591-4628
  • Source
    USFDA
29 más