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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 POROUS FEMORAL WEDGE SIZE 6 LARGE
Smith & Nephew, Inc.
71500062
Not in Commercial Distribution

  • 03596010218230 ()
71500062

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 6 SMALL
Smith & Nephew, Inc.
71500061
Not in Commercial Distribution

  • 03596010218223 ()
71500061

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S5 LARGE
Smith & Nephew, Inc.
71500054
Not in Commercial Distribution

  • 03596010218216 ()
71500054

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S5 SMALL
Smith & Nephew, Inc.
71500053
Not in Commercial Distribution

  • 03596010218209 ()
71500053

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 5 LARGE
Smith & Nephew, Inc.
71500052
Not in Commercial Distribution

  • 03596010218193 ()
71500052

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 5 SMALL
Smith & Nephew, Inc.
71500051
Not in Commercial Distribution

  • 03596010218186 ()
71500051

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S4 LARGE
Smith & Nephew, Inc.
71500044
Not in Commercial Distribution

  • 03596010218179 ()
71500044

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S4 SMALL
Smith & Nephew, Inc.
71500043
Not in Commercial Distribution

  • 03596010218162 ()
71500043

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 4 LARGE
Smith & Nephew, Inc.
71500042
Not in Commercial Distribution

  • 03596010218155 ()
71500042

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 4 SMALL
Smith & Nephew, Inc.
71500041
Not in Commercial Distribution

  • 03596010218148 ()
71500041

  • Knee arthroplasty wedge
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