Device Recall Color Cuff

Manufacturer

  • Manufacturer Address
    Stryker Instruments Div. of Stryker Corporation, 4100 E Milham Ave, Portage MI 49002-9704
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    Catalog No DT-7034-02-QC, Lot No 135905.
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Class II Recall - Nationwide Distribution.
  • Product Description
    Color Cuff II, Double Port Single Bladder - Reprocessed Sterile device -- Pneumatic tourniquet.
  • Manufacturer