SEARCH RESULTS FOR: Femoral(186009 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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JOURNEY FEMORAL SIZING STYLUS
Smith & Nephew, Inc.
E0017277-1
In Commercial Distribution

  • 00885556802502 ()
E0017277-1

  • Orthopaedic prosthesis implantation positioning instrument, reusable
JOURNEY FEMORAL SIZING STYLUS
Smith & Nephew, Inc.
E0017275-1
In Commercial Distribution

  • 00885556802465 ()
E0017275-1

  • Orthopaedic prosthesis implantation positioning instrument, reusable
2MM FEMORAL RECUT BLOCK
Smith & Nephew, Inc.
E0017257-1
In Commercial Distribution

  • 00885556801444 ()
E0017257-1

  • Osteotomy guide, reusable
2MM FEMORAL RECUT BLOCK
Smith & Nephew, Inc.
E0017256-1
In Commercial Distribution

  • 00885556801406 ()
E0017256-1

  • Osteotomy guide, reusable
4MM FEMORAL RECUT BLOCK
Smith & Nephew, Inc.
E0017255-2
In Commercial Distribution

  • 00885556801390 ()
E0017255-2

  • Osteotomy guide, reusable
2MM FEMORAL RECUT BLOCK
Smith & Nephew, Inc.
E0017255-1
In Commercial Distribution

  • 00885556801383 ()
E0017255-1

  • Osteotomy guide, reusable
FEMORAL SIZING/DRILL GUIDE
Smith & Nephew, Inc.
E0017157-1
In Commercial Distribution

  • 00885556796139 ()
E0017157-1

  • Surgical implant template, reusable
JOURNEY FEMORAL SIZING STYLUS
Smith & Nephew, Inc.
E0017178-1
In Commercial Distribution

  • 00885556796009 ()
E0017178-1

  • Orthopaedic prosthesis implantation positioning instrument, reusable
2MM FEMORAL RECUT BLOCK
Smith & Nephew, Inc.
E0017149-1
In Commercial Distribution

  • 00885556795248 ()
E0017149-1

  • Osteotomy guide, reusable
ANGIO DRAPE - FEMORAL, 1-EACH
Microtek Medical LLC
1
In Commercial Distribution

  • 50748426006118 ()
  • 00748426006113 ()


  • Angiographic drape
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