SEARCH RESULTS FOR: ("安卓應用加密[Contact Telegram: Heimaapp].ucb")(23886 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 SZ5-6 5MMXSHORT
Smith & Nephew, Inc.
71430704
In Commercial Distribution

  • 03596010212931 ()
71430704

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ3-4 5MMXSHORT
Smith & Nephew, Inc.
71430702
In Commercial Distribution

  • 03596010212924 ()
71430702

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ1-2 5MMXSHORT
Smith & Nephew, Inc.
71430700
In Commercial Distribution

  • 03596010212917 ()
71430700

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ7-8 10MMSHORT
Smith & Nephew, Inc.
71430698
In Commercial Distribution

  • 03596010212900 ()
71430698

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ5-6 10MMSHORT
Smith & Nephew, Inc.
71430696
In Commercial Distribution

  • 03596010212894 ()
71430696

  • Knee arthroplasty wedge
GEN II POSTERIOR FEM WEDGE TRIAL SZ3-4 10MMSHORT
Smith & Nephew, Inc.
71430694
In Commercial Distribution

  • 03596010212887 ()
71430694

  • Knee arthroplasty wedge
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
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