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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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No Description
Biomet Orthopedics, LLC
110018727
In Commercial Distribution

  • 00880304679122 ()

  • 14MM X 300MM
110018727

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018726
In Commercial Distribution

  • 00880304679115 ()

  • 13MM X 300MM
110018726

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018725
In Commercial Distribution

  • 00880304679108 ()

  • 12MM X 300MM
110018725

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018724
In Commercial Distribution

  • 00880304679092 ()

  • 11MM X 300MM
110018724

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018723
In Commercial Distribution

  • 00880304679085 ()

  • 18MM X 225MM
110018723

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018722
In Commercial Distribution

  • 00880304679078 ()

  • 17MM X 225MM
110018722

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018721
In Commercial Distribution

  • 00880304679061 ()

  • 16MM X 225MM
110018721

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018720
In Commercial Distribution

  • 00880304679054 ()

  • 15MM X 225MM
110018720

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018719
In Commercial Distribution

  • 00880304679047 ()

  • 14MM X 225MM
110018719

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
110018718
In Commercial Distribution

  • 00880304679030 ()

  • 13MM X 225MM
110018718

  • Knee femur prosthesis trial, reusable
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