SEARCH RESULTS FOR: ("源头企业签名[Contact Telegram: duo785].hfs")(12124 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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GEN II POSTERIOR FEM WEDGE TRIAL SZ7-8 5MMSHORT
Smith & Nephew, Inc.
71430692
In Commercial Distribution

  • 03596010212870 ()
71430692

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ5-6 5MMSHORT
Smith & Nephew, Inc.
71430690
In Commercial Distribution

  • 03596010212863 ()
71430690

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ3-4 5MMSHORT
Smith & Nephew, Inc.
71430688
In Commercial Distribution

  • 03596010212856 ()
71430688

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ1-2 5MM SHORT
Smith & Nephew, Inc.
71430686
In Commercial Distribution

  • 03596010212849 ()
71430686

  • Knee arthroplasty wedge
GNS II POSTERIOR FEM WEDGE TRIAL SZ7-8 5MM LONG
Smith & Nephew, Inc.
71430684
In Commercial Distribution

  • 03596010212832 ()
71430684

  • Knee arthroplasty wedge
GNS II POSTERIOR FEM WEDGE TRIAL SZ5-6 5MM LONG
Smith & Nephew, Inc.
71430682
In Commercial Distribution

  • 03596010212825 ()
71430682

  • Knee arthroplasty wedge
GNS II POSTERIOR FEM WEDGE TRIAL SZ3-4 5MM LONG
Smith & Nephew, Inc.
71430680
In Commercial Distribution

  • 03596010212818 ()
71430680

  • Knee arthroplasty wedge
GNS II POSTERIOR FEM WEDGE TRIAL SZ1-2 5MM LONG
Smith & Nephew, Inc.
71430678
In Commercial Distribution

  • 03596010212801 ()
71430678

  • Knee arthroplasty wedge
GENESIS II STACKED DISTAL L-WEDGE TRIAL SIZE 8
Smith & Nephew, Inc.
71430677
In Commercial Distribution

  • 03596010212795 ()
71430677

  • Knee arthroplasty wedge
GENESIS II STACKED DISTAL L-WEDGE TRIAL SIZE 7
Smith & Nephew, Inc.
71430676
In Commercial Distribution

  • 03596010212788 ()
71430676

  • Knee arthroplasty wedge
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