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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 Class Implantable

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SpheRx® DBR® III Rod, 120mm Pre-Bent
Nuvasive, Inc.
7217120
In Commercial Distribution

  • 00887517433497 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 110mm Pre-Bent
Nuvasive, Inc.
7217110
In Commercial Distribution

  • 00887517433480 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 105mm Pre-Bent
Nuvasive, Inc.
7217105
In Commercial Distribution

  • 00887517433473 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 100mm Pre-Bent
Nuvasive, Inc.
7217100
In Commercial Distribution

  • 00887517433466 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 95mm Pre-Bent
Nuvasive, Inc.
7217095
In Commercial Distribution

  • 00887517433459 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 90mm Pre-Bent
Nuvasive, Inc.
7217090
In Commercial Distribution

  • 00887517433442 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 85mm Pre-Bent
Nuvasive, Inc.
7217085
In Commercial Distribution

  • 00887517433435 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 80mm Pre-Bent
Nuvasive, Inc.
7217080
In Commercial Distribution

  • 00887517433428 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 75mm Pre-Bent
Nuvasive, Inc.
7217075
In Commercial Distribution

  • 00887517433411 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Tap, 7.0mm Solid Short
Nuvasive, Inc.
10000666
In Commercial Distribution

  • 00887517512888 ()


  • Bone tap, reusable
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