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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 S2 SMALL
Smith & Nephew, Inc.
71520023
Not in Commercial Distribution

  • 03596010227966 ()
71520023

  • 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 2 SMALL
Smith & Nephew, Inc.
71520021
Not in Commercial Distribution

  • 03596010227942 ()
71520021

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S1 LARGE
Smith & Nephew, Inc.
71520014
Not in Commercial Distribution

  • 03596010227935 ()
71520014

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S1 SMALL
Smith & Nephew, Inc.
71520013
Not in Commercial Distribution

  • 03596010227928 ()
71520013

  • Knee arthroplasty wedge
PROFIX TIBIAL WEDGE RESECTION GUIDE
Smith & Nephew, Inc.
71514513
Not in Commercial Distribution

  • 03596010224743 ()
71514513

  • Knee arthroplasty wedge
PROFIX POST/STAB FEMORAL WEDGE SPACER SZ7 LARGE
Smith & Nephew, Inc.
71512491
In Commercial Distribution

  • 23596010224235 ()
  • 03596010224231 ()
71512491

  • Knee arthroplasty wedge
PROFIX POST/STAB FEMORAL WEDGE SPACER SZ7 SMALL
Smith & Nephew, Inc.
71512490
In Commercial Distribution

  • 23596010224228 ()
  • 03596010224224 ()
71512490

  • Knee arthroplasty wedge
PROFIX POST/STAB FEMORAL WEDGE SPACER SZ6 LARGE
Smith & Nephew, Inc.
71512489
In Commercial Distribution

  • 23596010224211 ()
  • 03596010224217 ()
71512489

  • Knee arthroplasty wedge
PROFIX POST/STAB FEMORAL WEDGE SPACER SZ6 SMALL
Smith & Nephew, Inc.
71512488
In Commercial Distribution

  • 23596010224204 ()
  • 03596010224200 ()
71512488

  • Knee arthroplasty wedge
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