Altair

  • 모델명 / 제조번호(시리얼번호)
    55200-EU, 55200-GB, 55210-EU, 55210-GB, 55220-EU, 55220-GB | see FSN
  • 제품 설명
    MD: Stationary patient lifting system, line-powered
  • Manufacturer
  • 1 Event

제조사

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 26 건

데이터에 대해 더 자세히 알아보기 여기

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    md
  • Manufacturer
  • 모델명 / 제조번호(시리얼번호)
    Serial numbers: L001 to L191.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Direct accounts located in AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI.
  • 제품 설명
    Altaire, Magnetic Resonance Imaging Device.
  • Manufacturer
  • 모델명 / 제조번호(시리얼번호)
    L001 thru L182.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    The product was distributed throughout the United States and to one consignee located in both Wales and London.
  • 제품 설명
    Hitachi Altaire Magnetic Resonance Imaging Device.
  • Manufacturer
  • 모델명 / 제조번호(시리얼번호)
    L001 thru L223.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide-The device was distributed to consignees located throughout the United States.
  • 제품 설명
    Hitachi Altaire Magnetic Resonance Imaging System
  • Manufacturer
  • 모델명 / 제조번호(시리얼번호)
    L001-L225 - Altaire  C001-C693* - AIRIS II C701-C790 - AIRIS II Upgrades  H001-H091 - AIRIS Elite  H701-H748* - AIRIS Elite Upgrades   *The firm informed CIN-DO in their status reports for May, 2006 and again in August, 2007, that duplication was found in the number of system units originally reported to CIN-DO in early 2006. Ten (10) of the AIRIS II System units had been previously upgraded to AIRIS Elite units [System Unit Numbers: C012, C014, C032, C063, C111, C138, C263, C347, and C495] and are these numbers are reflected in the total # of AIRIS Elite System Unit Numbers listed above*  **By the same token, *eight (8) AIRIS Elite Upgrades [System ID Numbers: H735, H736, H740, H743, H745, H746, H747 & H748] were reportedly installed well after the corrective action was underway (7/28/06 to 11/24/2006) and were not-subject to corrective action. As a result, the total # of affected system units/customers has been revised to reflect the number reported by the firm [1129] beginning with their May, 2006 status report and continuing through to their final communication to CIN-DO dated 8/21/2007. - clp
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide
  • 제품 설명
    Magnetic Resonance Imaging Device
  • Manufacturer
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