Altair

  • Model / Serial
    55200-EU, 55200-GB, 55210-EU, 55210-GB, 55220-EU, 55220-GB | see FSN
  • Product Description
    MD: Stationary patient lifting system, line-powered
  • Manufacturer
  • 1 Event

Manufacturer

26 devices with a similar name

Learn more about the data here

  • Model / Serial
    Serial numbers: L001 to L191.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    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.
  • Product Description
    Altaire, Magnetic Resonance Imaging Device.
  • Manufacturer
  • Model / Serial
    L001 thru L182.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The product was distributed throughout the United States and to one consignee located in both Wales and London.
  • Product Description
    Hitachi Altaire Magnetic Resonance Imaging Device.
  • Manufacturer
  • Model / Serial
    L001 thru L223.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide-The device was distributed to consignees located throughout the United States.
  • Product Description
    Hitachi Altaire Magnetic Resonance Imaging System
  • Manufacturer
  • Model / Serial
    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
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    Magnetic Resonance Imaging Device
  • Manufacturer
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