Eluting Coronary Stent System

Fabricante

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    Biotronik told ICIJ that, when it identifies the need to issue a recall, the company immediately informs physicians of all potentially affected patients. It also noted that product recalls for all manufactures are publically available on the relevant national authorities’ websites. “As soon as an event is deemed serious either by a hospital or a manufacturer, it is reported inter alia to the regulatory authority in the country in which the incidence has occurred, as well as to the FDA for US-approved devices, even if the event has occurred outside of the US,” the company said.
  • Source
    DH

18 dispositivos con un nombre similar

Más información acerca de la data acá

  • Modelo / Serial
    Model: BMXP-3511, BMXP-3518, BMXP-4018, BMXP-4024, Affected: Batches: W15100548 W15100236 W15100237 W15100238 W15110086 W15120234
  • Manufacturer
  • Modelo / Serial
    Device Name : Orsiro Size : 2.75/40 REF number : 391240 LOT : 02152670, 02152671 Device Name : Orsiro Size : 3.0/40 REF number : 391241 LOT : 02152672, 02152673
  • Descripción del producto
    Stent System
  • Manufacturer
  • Modelo / Serial
  • ¿Implante?
    Yes
  • Descripción del producto
    Non-active implants
  • Manufacturer
  • Modelo / Serial
  • ¿Implante?
    Yes
  • Descripción del producto
    Non-active implants - special implants
  • Manufacturer
  • Modelo / Serial
  • ¿Implante?
    Yes
  • Descripción del producto
    Non-active implants - special implants
  • Manufacturer
13 más