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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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SpheRx® II Hook, Narrow Left Offset
Nuvasive, Inc.
7241125
In Commercial Distribution

  • 00887517443588 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Lamina Hook, 8mm Ext Narrow
Nuvasive, Inc.
7241120
In Commercial Distribution

  • 00887517443533 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Hook, 8mm Reduced Tip Wide
Nuvasive, Inc.
7241114
In Commercial Distribution

  • 00887517443175 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Hook, 8mm Reduced Tip Narrow
Nuvasive, Inc.
7241111
In Commercial Distribution

  • 00887517443144 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 80mm Dual Ball
Nuvasive, Inc.
7237800
In Commercial Distribution

  • 00887517439475 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 70.0mm DB Pre-Bent
Nuvasive, Inc.
7237700
In Commercial Distribution

  • 00887517439437 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 67.5mm DB Pre-Bent
Nuvasive, Inc.
7237675
In Commercial Distribution

  • 00887517439420 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 62.5mm DB Pre-Bent
Nuvasive, Inc.
7237625
In Commercial Distribution

  • 00887517439406 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 60.0mm DB Pre-Bent
Nuvasive, Inc.
7237600
In Commercial Distribution

  • 00887517439093 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 52.5mm DB Pre-Bent
Nuvasive, Inc.
7237525
In Commercial Distribution

  • 00887517439062 ()


  • Bone-screw internal spinal fixation system, non-sterile
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