MOMENTUM CRT-D

Fabricant

  • 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
    SATP

4 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    Model: , Affected: Model G124, G125, G126, G128
  • Manufacturer
  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Boston Scientific RESONATE, VIGILANT X4, PERCIVA, and MOMENTUM CRT-D/ICD
  • Manufacturer
  • Modèle / numéro de série
    VALITUDE CRT-PModel U128ARTG 279333RESONATE CRT-DModel G447ARTG 296562MOMENTUM CRT-DModel G124, G125, G126, G128ARTG 296563, 296564, 296565, 296566AUTOGEN CRT-DModels G172, G173, G175, G177, G179ARTG 221615, 221616, 221617, 221618, 221633VISIONIST CRT-PModels U225, U226, U228ARTG 279330, 279331, 279332DYNAGEN CRT-DModels G151, G156, G158ARTG 221620, 221621, 221622
  • Classification du dispositif
  • Manufacturer