Boston Scientific Cork LTD

5 dispositifs dans la base de données

  • Modèle / numéro de série
    see list | see list
  • Description du dispositif
    MD: Infusion catheter
  • Modèle / numéro de série
    M001171060, M001171080 M001171100, M001171120
  • Description du dispositif
    MD: Balloon catheter
  • Modèle / numéro de série
    M00354901520,M00354902020 M00354903020,M00355901020 M00355902020,M00355903020
  • Description du dispositif
    MD: Infusion catheter
  • Modèle / numéro de série
  • Description du dispositif
    MD: Infusion catheter
  • Modèle / numéro de série
    and Lot: see letter
  • Description du dispositif
    MD: Infusion catheter

Un fabricant avec un nom similaire

En savoir plus sur les données ici

  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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
    VNSAWH