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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ATTUNE KNEE SYSTEM REVISION FEMORAL CTT TRIAL RIGHT SIZE 6
DEPUY (IRELAND)
2504-40-206
In Commercial Distribution

  • 10603295439790 ()
250440206

  • Knee femur prosthesis trial, reusable
ATTUNE KNEE SYSTEM REVISION FEMORAL CTT TRIAL RIGHT SIZE 5
DEPUY (IRELAND)
2504-40-205
In Commercial Distribution

  • 10603295439776 ()
250440205

  • Knee femur prosthesis trial, reusable
ATTUNE KNEE SYSTEM REVISION FEMORAL CTT TRIAL LEFT SIZE 4
DEPUY (IRELAND)
2504-40-104
In Commercial Distribution

  • 10603295439745 ()
250440104

  • Knee femur prosthesis trial, reusable
ATTUNE KNEE SYSTEM REVISION FEMORAL CTT TRIAL RIGHT SIZE 3
DEPUY (IRELAND)
2504-40-203
In Commercial Distribution

  • 10603295439738 ()
250440203

  • Knee femur prosthesis trial, reusable
ATTUNE KNEE SYSTEM REVISION FEMORAL CTT TRIAL LEFT SIZE 3
DEPUY (IRELAND)
2504-40-103
In Commercial Distribution

  • 10603295439721 ()
250440103

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
32-360271
In Commercial Distribution

  • 00880304499980 ()
32-360271

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
32-360272
In Commercial Distribution

  • 00880304499942 ()
32-360272

  • Knee femur prosthesis trial, reusable
LCS Completion REVISION FEMORAL IM PLATE RIGHT
DEPUY ORTHOPAEDICS, INC.
2178-61-092
In Commercial Distribution

  • 10603295095996 ()
217861092

  • Knee femur prosthesis trial, reusable
LCS Completion REVISION FEMORAL IM PLATE LEFT
DEPUY ORTHOPAEDICS, INC.
2178-61-090
In Commercial Distribution

  • 10603295095989 ()
217861090

  • Knee femur prosthesis trial, reusable
LCS Completion REV FEMORAL AUG BUTTON 15MM DISTAL STD+/LG+
DEPUY ORTHOPAEDICS, INC.
2178-60-086
In Commercial Distribution

  • 10603295095835 ()
217860086

  • Knee femur prosthesis trial, reusable
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