SEARCH RESULTS FOR: ("源头企业签名[Contact Telegram: duo785].hfs")(12056 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 5MMSHORT
Smith & Nephew, Inc.
71430690
In Commercial Distribution

  • 03596010212863 ()
71430690

  • 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 SZ1-2 5MM LONG
Smith & Nephew, Inc.
71430678
In Commercial Distribution

  • 03596010212801 ()
71430678

  • Knee arthroplasty wedge
GENESIS II FULL TIBIAL WEDGE SZ7 7DEGREE TRIAL
Smith & Nephew, Inc.
71430013
In Commercial Distribution

  • 03596010211071 ()
71430013

  • Knee arthroplasty wedge
GENESIS II FULL TIBIAL WEDGE SZ 5 7DEGREE TRIAL
Smith & Nephew, Inc.
71430009
In Commercial Distribution

  • 03596010211040 ()
71430009

  • Knee arthroplasty wedge
GENESIS II FULL TIBIAL WEDGE SIZE 3 7 DEG TRIAL
Smith & Nephew, Inc.
71430005
In Commercial Distribution

  • 03596010211019 ()
71430005

  • Knee arthroplasty wedge
GENESIS II FULL TIBIAL WEDGE SIZE1 7DEGREE TRIAL
Smith & Nephew, Inc.
71430001
In Commercial Distribution

  • 03596010210982 ()
71430001

  • Knee arthroplasty wedge
GENESIS II TIBIAL FINNED FIXATION PEG SIZE 7-8
Smith & Nephew, Inc.
71420996
In Commercial Distribution

  • 03596010210289 ()
71420996

  • Knee arthroplasty wedge
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