Devices

Femoral Compression Device

  • Model / Serial
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, MA, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, WA, WI, and WV OUS: CANADA
  • Product Description
    Femoral Compression Device || Model #'s: || RAD11163 || Intended for use in the compression of the femoral artery or vein after cauterization.
  • Manufacturer
    Sterilmed Inc
  • 1 Event

Manufacturer

Sterilmed Inc
  • Manufacturer Address
    Sterilmed Inc, 11400 73rd Ave N Ste 100, Osseo MN 55369-5562
  • Manufacturer Parent Company (2017)
    Johnson & Johnson
  • Source
    USFDA

One device with a similar name

Learn more about the data here

Device Recall FemoStop Reprocessed Femoral Compression Device
  • Model / Serial
    Lot: 869509, 878402, 878439, 879762, 879990, 880274.
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Devices were distributed to 8 consignees (end users/hospitals) located in VA, CA, FL, MI, WA.
  • Product Description
    ASCENT HEALTHCARE SOLUTIONS. Reprocessed Femoral Compression Device, Model 11165.
  • Manufacturer
    Ascent Healthcare Solutions, Inc.