PneumoSure High Flow Insufflator

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
    DH

3 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
  • Description du dispositif
    Class IIB
  • Manufacturer
  • Modèle / numéro de série
  • Description du dispositif
    PneumoSure High Flow Insufflator High Pressure Unit, Stryker Endoscopy
  • Manufacturer
  • Modèle / numéro de série
    620-040-600, 620-040-601, 620-040-602, 620-040-604, 620-040-610, 620-040-611, 620-040-613, 620-040-614, 2400069 | see FSN
  • Description du dispositif
    MD: Laparoscopic insufflator
  • Manufacturer