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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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LIF, RASP, CC OFFSET, 20MM
ALPHATEC SPINE, INC.
256-16-100-20
In Commercial Distribution

  • 00190376394404 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 18MM
ALPHATEC SPINE, INC.
256-16-100-18
In Commercial Distribution

  • 00190376394398 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 16MM
ALPHATEC SPINE, INC.
256-16-100-16
In Commercial Distribution

  • 00190376394381 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 14MM
ALPHATEC SPINE, INC.
256-16-100-14
In Commercial Distribution

  • 00190376394374 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 12MM
ALPHATEC SPINE, INC.
256-16-100-12
In Commercial Distribution

  • 00190376394367 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 10MM
ALPHATEC SPINE, INC.
256-16-100-10
In Commercial Distribution

  • 00190376394350 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 24MM
ALPHATEC SPINE, INC.
256-16-100-24
In Commercial Distribution

  • 00190376393223 ()


  • Bone file/rasp, manual, reusable
110mm C-C Blade, Sigma TLIF
ALPHATEC SPINE, INC.
269-150-110
In Commercial Distribution

  • 00190376316598 ()


  • Surgical retraction system, reusable
100mm C-C Blade, Sigma TLIF
ALPHATEC SPINE, INC.
269-150-100
In Commercial Distribution

  • 00190376316581 ()


  • Surgical retraction system, reusable
80mm C-C Blade, Sigma TLIF
ALPHATEC SPINE, INC.
269-150-080
In Commercial Distribution

  • 00190376316567 ()


  • Surgical retraction system, reusable
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