SEARCH RESULTS FOR: ("源头企业签名[Contact Telegram: duo785].hfs")(4912 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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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
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
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