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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 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
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S3 LARGE
Smith & Nephew, Inc.
71500034
Not in Commercial Distribution

  • 03596010218131 ()
71500034

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S3 SMALL
Smith & Nephew, Inc.
71500033
Not in Commercial Distribution

  • 03596010218124 ()
71500033

  • Knee arthroplasty wedge
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 DISTAL ONLY FEMORAL WEDGE S2 LARGE
Smith & Nephew, Inc.
71500024
Not in Commercial Distribution

  • 03596010218094 ()
71500024

  • Knee arthroplasty wedge
PROFIX FEMORAL WEDGE SIZE 2 LARGE
Smith & Nephew, Inc.
71500022
Not in Commercial Distribution

  • 03596010218070 ()
71500022

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

  • 03596010218063 ()
71500021

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ7-8 10MMXSHRT
Smith & Nephew, Inc.
71430712
In Commercial Distribution

  • 03596010212979 ()
71430712

  • Knee arthroplasty wedge
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