Device Recall Terumo Perfusion System 8000

Manufacturer

  • Manufacturer Address
    Terumo Cardiovascular Systems Corp, 6200 Jackson Rd, Ann Arbor MI 48103-9586
  • Source
    USFDA

4 devices with a similar name

Learn more about the data here

  • Model / Serial
    Hand crank serial numbers 1197 through 1214.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Belgium, Hong Kong, Japan, Taiwan and United Arab Emirates.
  • Product Description
    Terumo Perfusion System 8000 Base, 5 pump, 220/240v; Model 8000; Catalog No. 16406.
  • Manufacturer
  • Model / Serial
    Hand crank serial numbers 1621 and 1622.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Belgium, Hong Kong, Japan, Taiwan and United Arab Emirates.
  • Product Description
    Terumo Perfusion System 8000 Base, 5 pump, 100v, Model 8000; Catalog No. 16410.
  • Manufacturer
  • Model / Serial
    Hand crank serial numbers 1240 through 1247.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Belgium, Hong Kong, Japan, Taiwan and United Arab Emirates.
  • Product Description
    Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 8000; Catalog No. 16400.
  • Manufacturer
  • Model / Serial
    Hand crank serial numbers 1963 through 1986.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Belgium, Hong Kong, Japan, Taiwan and United Arab Emirates.
  • Product Description
    Terumo Perfusion System 8000 Base, 5 pump, 115v; Model 8000; Catalog No. 16401.
  • Manufacturer