Boston Scientific Corporation

15 dispositifs dans la base de données

  • Modèle / numéro de série
    Model Number: Maestro 4000 Footswitch: M004218500- Maestro 4000 Footswitch M00421850D0- Maestro 4000 Footswitch, Demo M00421850H0- Maestro 4000 Footswitch, Hospital Owned M00421850R0- Maestro 4000 Footswitch, Repaired M00421850Z0- Maestro 4000 Footswitch, Zero Cost Maestro Pump to Generator Cable: M004315000- Cable OI Pump to OI Maestro Maestro 4000 Controller: M00440000- Maestro 4000 Controller M0044000D0- Maestro 4000 Controller, Demo M0044000H0- Maestro 4000 Controller, Hospital Owned M0044000R0- Maestro 4000 Controller, Repaired M0044000Z0- Maestro 4000 Controller, Zero Cost
  • Description du dispositif
    Electromechanical medical devices
  • Modèle / numéro de série
    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
  • Description du dispositif
    Inactive implantable medical devices
  • Modèle / numéro de série
    Catalog Number: M003101430, M003101440, M003101470, M003101480, M003101510, M003101520, H965100430, H965100440, H965100470, H965100480, H965100510, H965100520
  • Description du dispositif
    Medical devices for single use
  • Modèle / numéro de série
    Catalog Number: M00546600 Batch Number: viz FSN
  • Description du dispositif
    Medical devices for single use
  • Modèle / numéro de série
    Model Number: ELUVIA H74939295601570, H74939295601510, H74939295701570, H74939295701510 Innova (Class IIb, GMDN 47932: Multiple Peripheral Artery Stent , Commercial name: Innova ™ Over the Wire Self-Expanding Stent) H74939180051870, H74939180052070, H74939180061870, H74939180062070, H74939180071870, H74939180072070, H74939180081870, H74939180082070, H74939181051830, H74939181052030, H74939181061830, H74939181062030, H74939181071830, H74939181072030, H74939181081830, H74939181082030
  • Description du dispositif
    Inactive implantable medical devices
10 en plus

63 fabricants 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
    TDMDAT
  • 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
    NIDFSINVIMA
  • 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
    NIDFSINVIMA
  • 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
    NIDFSINVIMA
  • 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
    AMPMDC
58 en plus