COVIDIEN

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 55 건

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 4-070550-SP (Lot serial: ); Model Catalog: 4-840120DICU-EN (Lot serial: )
  • 의료기기 분류등급
  • 제품 설명
    PURITAN BENNETT 840 VENTILATOR
  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: CTRF117 (Lot serial: C5C176C)
  • 제품 설명
    RADIONICS COOL-TIP RF SYSTEM
  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: (Lot serial: N5L235K AND LOWER); Model Catalog: (Lot serial: N5L247K AND LOWER)
  • 제품 설명
    LIGASURE ATLAS LS1120
  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: SWCT15303 (Lot serial: >10 see with manufacturer); Model Catalog: SWCT1530 (Lot serial: >10 see with manufacturer); Model Catalog: ACTC2025 (Lot serial: >10 see with manufacturer); Model Catalog: ACTC1525 (Lot serial: >10 see with manufacturer); Model Catalog: ACTC1025 (Lot serial: >10 see with manufacturer); Model Catalog: ACT2530 (Lot serial: >10 see with manufacturer); Model Catalog: ACT2030 (Lot serial: >10 see with manufacturer); Model Catalog: ACT2020 (Lot serial: >10 see with manufacturer); Model Catalog: ACT1530 (Lot serial: >10 see with manufacturer); Model Catalog: ACT1520 (Lot serial: >10 see with manufacturer); Model Catalog: ACT1510 (Lot serial: >10 see with manufacturer); Model Catalog: ACT1507 (Lot serial: >10 see with manufacturer); Model Catalog: ACT1030 (Lot serial: >10 see with manufacturer); Model Catalog: ACT1020 (Lot serial: >10 see with manufacturer); Model Catalog: SWCT1540 (Lot serial: >10 see with manufacturer); Model Catalog: SWCT2530 (Lot serial: >10 see with manufa
  • 의료기기 분류등급
  • 제품 설명
    COOL-TIP RF SINGLE ELECTRODE KIT
  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 980U1ENDICU (Lot serial: S/N: >10 CONTACT MFR)
  • 의료기기 분류등급
  • 제품 설명
    PURITAN BENNETT 980 SERIES VENTILATOR
하나 더 50 건 더

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 179 건

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 모회사 (2017)
  • 제조사 의견
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    TDMDAT
  • 제조사 모회사 (2017)
  • 제조사 의견
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    TDMDAT
  • 제조사 모회사 (2017)
  • 제조사 의견
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    NIDFSINVIMA
  • 제조사 모회사 (2017)
  • 제조사 의견
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    NIDFSINVIMA
  • 제조사 모회사 (2017)
  • 제조사 의견
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    NIDFSINVIMA
하나 더 174 건 더