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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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4mm KERRISON 90 DEG. BAYONETED, W/O Tang
ALPHATEC SPINE, INC.
CI-11425-71
In Commercial Distribution

  • 00840180522158 ()


  • Spinal rongeur
3mm KERRISON 90 DEG. BAYONETED, W/O Tang
ALPHATEC SPINE, INC.
CI-11425-70
In Commercial Distribution

  • 00840180522141 ()


  • Spinal rongeur
2mm KERRISON 90 DEG. BAYONETED, W/O Tang
ALPHATEC SPINE, INC.
CI-11425-69
In Commercial Distribution

  • 00840180522134 ()


  • Spinal rongeur
4mm KERRISON 40 DEG. BAYONETED, W/O Tang
ALPHATEC SPINE, INC.
CI-11425-67
In Commercial Distribution

  • 00840180522127 ()


  • Spinal rongeur
2mm KERRISON 40 DEG. BAYONETED, W/O Tang
ALPHATEC SPINE, INC.
CI-11425-65
In Commercial Distribution

  • 00840180522110 ()


  • Spinal rongeur
5mm KERRISON 40 DEG. BAYONETED, W/O Tang
ALPHATEC SPINE, INC.
CI-11425-68
In Commercial Distribution

  • 00840180522103 ()


  • Spinal rongeur
2mm LIF Kerrison, 12"
ALPHATEC SPINE, INC.
CI-11324
In Commercial Distribution

  • 00840180518793 ()


  • Spinal rongeur
2mm LIF Pituitary, 12"
ALPHATEC SPINE, INC.
CI-11323
In Commercial Distribution

  • 00840180518786 ()


  • Spinal rongeur
5mm Up-biting Posterior Serrated Pituitary Rongeur, 8", Finger Loop
ALPHATEC SPINE, INC.
CI-11285-05-1
In Commercial Distribution

  • 00840180517048 ()


  • Spinal rongeur
5mm Straight Posterior Serrated Pituitary Rongeur, 8", Finger Loop
ALPHATEC SPINE, INC.
CI-11285-05-0
In Commercial Distribution

  • 00840180517031 ()


  • Spinal rongeur
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