offroad re-entry catheter system

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
    MSHM

5 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
  • Description du dispositif
    medical_device
  • Manufacturer
  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Boston Scientific OffRoad Re-Entry Catheter System
  • Manufacturer
  • Modèle / numéro de série
    392021 -0054 | 16458224, 16514006, 16514008,16805826, 16949014
  • Description du dispositif
    MD: Intravascular guiding catheter
  • Manufacturer
  • Modèle / numéro de série
    Model Catalog: H74939202070540 (Lot serial: 16458224); Model Catalog: H74939202070540 (Lot serial: 16514006); Model Catalog: H74939202070540 (Lot serial: 16949014); Model Catalog: H74939202070540 (Lot serial: 16805826); Model Catalog: H74939202070540 (Lot serial: 16514008)
  • Description du dispositif
    OffRoad Re-Entry Catheter System
  • Manufacturer