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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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PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S4 LARGE
Smith & Nephew, Inc.
71520044
Not in Commercial Distribution

  • 03596010228055 ()
71520044

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S4 SMALL
Smith & Nephew, Inc.
71520043
Not in Commercial Distribution

  • 03596010228048 ()
71520043

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 4 LARGE
Smith & Nephew, Inc.
71520042
Not in Commercial Distribution

  • 03596010228031 ()
71520042

  • 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 NONPOR DISTAL ONLY FEMORAL WEDGE S3 LARGE
Smith & Nephew, Inc.
71520034
Not in Commercial Distribution

  • 03596010228017 ()
71520034

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S3 SMALL
Smith & Nephew, Inc.
71520033
Not in Commercial Distribution

  • 03596010228000 ()
71520033

  • 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 3 LARGE
Smith & Nephew, Inc.
71520031
Not in Commercial Distribution

  • 03596010227980 ()
71520031

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S2 LARGE
Smith & Nephew, Inc.
71520024
Not in Commercial Distribution

  • 03596010227973 ()
71520024

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S2 SMALL
Smith & Nephew, Inc.
71520023
Not in Commercial Distribution

  • 03596010227966 ()
71520023

  • Knee arthroplasty wedge
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