SEARCH RESULTS FOR: ("安卓應用加密[Contact Telegram: Heimaapp].ucb")(12072 results)

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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 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
GENESIS II ANGLED/STEP WEDGE RESECTION GUIDE
Smith & Nephew, Inc.
71440280
Not in Commercial Distribution

  • 03596010214829 ()
71440280

  • Knee arthroplasty wedge
GNS II MEDIAL LATERAL TIB WEDGE TRIAL SIZE 7-8
Smith & Nephew, Inc.
71430752
In Commercial Distribution

  • 03596010213174 ()
71430752

  • Knee arthroplasty wedge
GNS II MEDIAL LATERAL TIB WEDGE TRIAL SIZE 5-6
Smith & Nephew, Inc.
71430750
In Commercial Distribution

  • 03596010213167 ()
71430750

  • Knee arthroplasty wedge
GNS II MEDIAL LATERAL TIB WEDGE TRIAL SIZE 3-4
Smith & Nephew, Inc.
71430748
In Commercial Distribution

  • 03596010213150 ()
71430748

  • Knee arthroplasty wedge
GNS II MEDIAL LATERAL TIB WEDGE TRIAL SIZE 1-2
Smith & Nephew, Inc.
71430746
In Commercial Distribution

  • 03596010213143 ()
71430746

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

  • 03596010212979 ()
71430712

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ5-6 10MMXSHRT
Smith & Nephew, Inc.
71430710
In Commercial Distribution

  • 03596010212962 ()
71430710

  • Knee arthroplasty wedge
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