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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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TYPHOON,DRILL,4.5,ADJUSTABLE,SOLID
Choice Spine, LP
K070-ASD45
In Commercial Distribution

  • 00840996131124 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,DRILL,4.5,ADJUSTABLE,SOLID
Choice Spine, LP
K070-ASD44
In Commercial Distribution

  • 00840996131117 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,MI,TAP,5.5,ADJUSTABLE,CANN
Choice Spine, LP
K070-ACT54
In Commercial Distribution

  • 00840996131100 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,MI,TAP,4.5,ADJUSTABLE,CANN
Choice Spine, LP
K070-ACT44
In Commercial Distribution

  • 00840996131094 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,MI,DRILL,5.5,ADJUSTABLE,CANN
Choice Spine, LP
K070-ACD54
In Commercial Distribution

  • 00840996131087 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,MI,DRILL,4.5,ADJUSTABLE,CANN
Choice Spine, LP
K070-ACD44
In Commercial Distribution

  • 00840996131070 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,MI,INITIAL DILATOR
Choice Spine, LP
K070-0021
In Commercial Distribution

  • 00840996131063 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,MI,GUIDEWIRE SLEEVE
Choice Spine, LP
K070-0020
In Commercial Distribution

  • 00840996131056 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,MI,SLAP HAMMER
Choice Spine, LP
K070-0019
In Commercial Distribution

  • 00840996131049 ()


  • Trans-facet-screw internal spinal fixation system, sterile
TYPHOON,MI,FINAL DILATOR
Choice Spine, LP
K070-0018
In Commercial Distribution

  • 00840996131032 ()


  • Trans-facet-screw internal spinal fixation system, sterile
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