SEARCH RESULTS FOR: ("源头企业签名[Contact Telegram: duo785].hfs")(23937 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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LEGION HEMI ANGLED WEDGE RESECTION GUIDE
Smith & Nephew, Inc.
71434343
Not in Commercial Distribution

  • 03596010549938 ()
71434343

  • 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
GEN II POSTERIOR FEM WEDGE TRIAL SZ3-4 10MMXSHRT
Smith & Nephew, Inc.
71430708
In Commercial Distribution

  • 03596010212955 ()
71430708

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ7-8 5MMXSHORT
Smith & Nephew, Inc.
71430706
In Commercial Distribution

  • 03596010212948 ()
71430706

  • Knee arthroplasty wedge
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