SEARCH RESULTS FOR: Femoral(210090 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Femoral Box Trial #12
Corentec Co., Ltd
KB.SFT.E12BB
In Commercial Distribution

  • 08800068965462 ()


  • Knee femur prosthesis trial, reusable
Femoral Box Trial #11
Corentec Co., Ltd
KB.SFT.E11BB
In Commercial Distribution

  • 08800068965455 ()


  • Orthopaedic prosthesis implantation positioning instrument, reusable
Femoral Box Trial #09
Corentec Co., Ltd
KB.SFT.E09BB
In Commercial Distribution

  • 08800068965448 ()


  • Knee femur prosthesis trial, reusable
Femoral Box Trial #07
Corentec Co., Ltd
KB.SFT.E07BB
In Commercial Distribution

  • 08800068965431 ()


  • Orthopaedic prosthesis implantation positioning instrument, reusable
Femoral Box Trial #05
Corentec Co., Ltd
KB.SFT.E05BB
In Commercial Distribution

  • 08800068965424 ()


  • Orthopaedic prosthesis implantation positioning instrument, reusable
Femoral Box Trial #04
Corentec Co., Ltd
KB.SFT.E04BB
In Commercial Distribution

  • 08800068965417 ()


  • Orthopaedic prosthesis implantation positioning instrument, reusable
Femoral Box Trial #03
Corentec Co., Ltd
KB.SFT.E03BB
In Commercial Distribution

  • 08800068965400 ()


  • Orthopaedic prosthesis implantation positioning instrument, reusable
Tiburon Femoral Angiography Drape
Cardinal Health 200, LLC
29520
In Commercial Distribution

  • 50885380141711 ()
  • 10885380141713 ()
29520

  • Angiographic drape
Radial/Femoral Angiography Sheet
Cardinal Health 200, LLC
D2388
Not in Commercial Distribution

  • 50885380058071 ()
  • 10885380058073 ()
D2388

  • Patient surgical drape, single-use
Tiburon Femoral Angiography Drape
Cardinal Health 200, LLC
29520
In Commercial Distribution

  • 50885380038073 ()
  • 10885380038075 ()
29520

  • Angiographic drape
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