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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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 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 3-4
Smith & Nephew, Inc.
71430748
In Commercial Distribution

  • 03596010213150 ()
71430748

  • 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 SZ3-4 10MMXSHRT
Smith & Nephew, Inc.
71430708
In Commercial Distribution

  • 03596010212955 ()
71430708

  • Knee arthroplasty wedge
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