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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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T'BOLT,KWIRE,NITOL,BLUNT-TROCAR,LASER,20
Choice Spine, LP
M070-LN220
In Commercial Distribution

  • 00840996173728 ()


  • Spinal guidewire
T'BOLT,KWIRE,NITOL,BLUNT-TROCAR,LASER,12
Choice Spine, LP
M070-LN212
In Commercial Distribution

  • 00840996173711 ()


  • Spinal guidewire
T'BOLT,KWIRE,NITOL,BLUNT-BLUNT,LASER,24
Choice Spine, LP
M070-LN124
In Commercial Distribution

  • 00840996173704 ()


  • Spinal guidewire
T'BOLT,KWIRE,NITOL,BLUNT-BLUNT,LASER,22
Choice Spine, LP
M070-LN122
In Commercial Distribution

  • 00840996173698 ()


  • Spinal guidewire
T'BOLT,KWIRE,NITOL,BLUNT-BLUNT,LASER,20
Choice Spine, LP
M070-LN120
In Commercial Distribution

  • 00840996173681 ()


  • Spinal guidewire
T'BOLT,KWIRE,NITOL,BLUNT-BLUNT,LASER,12
Choice Spine, LP
M070-LN112
In Commercial Distribution

  • 00840996173674 ()


  • Spinal guidewire
VEO,DISTRACTOR,PADDLE,22X0 DEG
Choice Spine, LP
V070-0112
In Commercial Distribution

  • 00840996173230 ()


  • Polymeric spinal interbody fusion cage
VEO,DISTRACTOR,PADDLE,17X0 DEG
Choice Spine, LP
V070-0111
In Commercial Distribution

  • 00840996173223 ()


  • Polymeric spinal interbody fusion cage
BLACKBIRD,TORQUE LIMITER
Choice Spine, LP
L070-0061
In Commercial Distribution

  • 00840996173216 ()


  • Orthopaedic implant driver
PLI,PARALLEL,PADDLE,SHAVER,7X3.25
Choice Spine, LP
P070-6062
In Commercial Distribution

  • 00840996171144 ()


  • Polymeric spinal interbody fusion cage
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