Boston Scientific Corporation

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 15 건

  • 모델명 / 제조번호(시리얼번호)
    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
  • 제품 설명
    Electromechanical medical devices
  • 모델명 / 제조번호(시리얼번호)
    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
  • 제품 설명
    Inactive implantable medical devices
  • 모델명 / 제조번호(시리얼번호)
    Catalog Number: M003101430, M003101440, M003101470, M003101480, M003101510, M003101520, H965100430, H965100440, H965100470, H965100480, H965100510, H965100520
  • 제품 설명
    Medical devices for single use
  • 모델명 / 제조번호(시리얼번호)
    Catalog Number: M00546600 Batch Number: viz FSN
  • 제품 설명
    Medical devices for single use
  • 모델명 / 제조번호(시리얼번호)
    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
  • 제품 설명
    Inactive implantable medical devices
하나 더 10 건 더

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 63 건

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 모회사 (2017)
  • 제조사 의견
    “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
  • 제조사 모회사 (2017)
  • 제조사 의견
    “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
  • 제조사 모회사 (2017)
  • 제조사 의견
    “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
  • 제조사 모회사 (2017)
  • 제조사 의견
    “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
  • 제조사 모회사 (2017)
  • 제조사 의견
    “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
하나 더 58 건 더