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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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PLI,SHAVER,PADDLE,QC,HUDSON,6
Choice Spine, LP
P070-2106
In Commercial Distribution

  • 00840996188609 ()


  • Polymeric spinal interbody fusion cage
PLI,SHAVER,PADDLE,QC,HUDSON,5
Choice Spine, LP
P070-2105
In Commercial Distribution

  • 00840996188593 ()


  • Polymeric spinal interbody fusion cage
PLI,SHAVER,PADDLE,QC,HUDSON,4
Choice Spine, LP
P070-2104
In Commercial Distribution

  • 00840996188586 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,12 DEG,22X17
Choice Spine, LP
V070-B122217
In Commercial Distribution

  • 00840996188067 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,12 DEG,22X15
Choice Spine, LP
V070-B122215
In Commercial Distribution

  • 00840996188050 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,12 DEG,22X13
Choice Spine, LP
V070-B122213
In Commercial Distribution

  • 00840996188043 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,12 DEG,22X11
Choice Spine, LP
V070-B122211
In Commercial Distribution

  • 00840996188036 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,12 DEG,22X9
Choice Spine, LP
V070-B122209
In Commercial Distribution

  • 00840996188029 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,12 DEG,17X17
Choice Spine, LP
V070-B121717
In Commercial Distribution

  • 00840996188012 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,12 DEG,17X15
Choice Spine, LP
V070-B121715
In Commercial Distribution

  • 00840996188005 ()


  • Polymeric spinal interbody fusion cage
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