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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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VEO,TRIAL,POLISHED,0 DEG,17X11
Choice Spine, LP
V070-01711P
In Commercial Distribution

  • 00840996170543 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,0 DEG,17X9
Choice Spine, LP
V070-01709P
In Commercial Distribution

  • 00840996170536 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,0 DEG,17X7.5
Choice Spine, LP
V070-01775P
In Commercial Distribution

  • 00840996170529 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,22X15
Choice Spine, LP
V070-A2215P
In Commercial Distribution

  • 00840996170512 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,22X13
Choice Spine, LP
V070-A2213P
In Commercial Distribution

  • 00840996170505 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,22X11
Choice Spine, LP
V070-A2211P
In Commercial Distribution

  • 00840996170499 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,22X9
Choice Spine, LP
V070-A2209P
In Commercial Distribution

  • 00840996170482 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,22X7.5
Choice Spine, LP
V070-A2275P
In Commercial Distribution

  • 00840996170475 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,17X15
Choice Spine, LP
V070-A1715P
In Commercial Distribution

  • 00840996170468 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,17X13
Choice Spine, LP
V070-A1713P
In Commercial Distribution

  • 00840996170451 ()


  • Polymeric spinal interbody fusion cage
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