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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PROFIX POROUS FEMORAL WEDFE SIZE 3 LARGE
Smith & Nephew, Inc.
71500032
Not in Commercial Distribution

  • 03596010218117 ()
71500032

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 3 SMALL
Smith & Nephew, Inc.
71500031
Not in Commercial Distribution

  • 03596010218100 ()
71500031

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 2 SMALL
Smith & Nephew, Inc.
71500021
Not in Commercial Distribution

  • 03596010218063 ()
71500021

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 6 LARGE
Smith & Nephew, Inc.
71520062
Not in Commercial Distribution

  • 03596010228116 ()
71520062

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 5 SMALL
Smith & Nephew, Inc.
71520051
Not in Commercial Distribution

  • 03596010228062 ()
71520051

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 4 SMALL
Smith & Nephew, Inc.
71520041
Not in Commercial Distribution

  • 03596010228024 ()
71520041

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 3 LARGE
Smith & Nephew, Inc.
71520032
Not in Commercial Distribution

  • 03596010227997 ()
71520032

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 2 LARGE
Smith & Nephew, Inc.
71520022
Not in Commercial Distribution

  • 03596010227959 ()
71520022

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 7 LARGE
Smith & Nephew, Inc.
71520072
Not in Commercial Distribution

  • 03596010228154 ()
71520072

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 7 SMALL
Smith & Nephew, Inc.
71520071
Not in Commercial Distribution

  • 03596010228147 ()
71520071

  • Knee arthroplasty wedge
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