Covidien Pty Ltd

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 45 건

  • 모델명 / 제조번호(시리얼번호)
    Solitaire Platinum Revascularisation DeviceProduct Codes: SRD3-4-20-10, SRD3-4- 40-10, SRD3-6-20-10 and SRD3-6-40-10ARTG Number: 284964
  • 모델명 / 제조번호(시리얼번호)
    Newport HT70 and HT70 Plus VentilatorsARTG Number: 14214
  • 의료기기 분류등급
  • 모델명 / 제조번호(시리얼번호)
    Covidien Curity Eye Pad, Curity Eye Pad Oval, Curity Sodium Chloride Dressing Covidien Curity Eye Pad Item Code: 03201Lot Numbers beginning with 12, 13, 14, 15 and16Covidien Curity Eye Pad OvalItem Code: 2841Lot Numbers beginning with 12, 13, 14, 15 and16Covidien Curity Sodium Chloride Dressing Item Code: 3339Lot Number beginning with 14, 15, 16 (Excluding lots: 16J098062, 16J098162, 16J098262)ARTG Numbers: 186368, 186373
  • 모델명 / 제조번호(시리얼번호)
    Valleylab Laparoscopic Handset, Four-FunctionItem Number: E2750Multiple Lot NumbersARTG Number: 178370
  • 의료기기 분류등급
  • 모델명 / 제조번호(시리얼번호)
    Covidien Devon Light Glove Product Codes: 571711, 31140208, 31140216, 31140257All Lot Numbers within expiry beginning with 630XXXXXXX and lower ARTG Number: 186761
하나 더 40 건 더

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 2 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.
  • 제조사 대표
    Allied Medical Group S.A.L - DIMA HEALTHCARE SA
  • Source
    RLMPH
  • 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.
  • 제조사 대표
    DIMA HEALTHCARE SA - Allied Medical Group S.A.L
  • Source
    RLMPH