Capio™ SLIM Suture Capturing Device,


  • 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.”
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  • Modelo / Serial
    Model Number: Capio™ SLIM Suture Capturing Device M0068318250 Capio™ SLIM Suture Capturing Device (Box 5) M0068318261 Capio™ Open Access Suture Capturing Device (Box 4) M0068311251 Capio™ Standard Suture Capturing Device (Box 4) M0068312321 Capio™ RP Suture Capturing Device M0068321010 Uphold™ LITE with Capio™ SLIM Vaginal Support System M0068318170 Pinnacle™ Anterior Pelvic Floor Repair Kit M0068317050 Pinnacle™ LITE Posterior with Capio SLIM Pelvic Floor Repair Kit M0068318150
  • Descripción del producto
    Inactive implantable medical devices
  • Manufacturer