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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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PRECEPT Ti Rod, 110mm Straight
Nuvasive, Inc.
8848110
In Commercial Distribution

  • 00887517379245 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Ti Rod, 100mm Straight
Nuvasive, Inc.
8848100
In Commercial Distribution

  • 00887517379238 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Ti Rod, 90mm Straight
Nuvasive, Inc.
8848090
In Commercial Distribution

  • 00887517379214 ()


  • Bone-screw internal spinal fixation system, non-sterile
CoRoent LO, 15x10x35mm 5°
Nuvasive, Inc.
6851512
In Commercial Distribution

  • 00887517379191 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 15x10x30mm 5°
Nuvasive, Inc.
6851511
In Commercial Distribution

  • 00887517379184 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 15x10x25mm 5°
Nuvasive, Inc.
6851510
In Commercial Distribution

  • 00887517379177 ()


  • Polymeric spinal interbody fusion cage
CoRoent LW, 14x10x35mm 5°
Nuvasive, Inc.
6851417
In Commercial Distribution

  • 00887517379160 ()


  • Polymeric spinal interbody fusion cage
CoRoent LW, 14x10x30mm 5°
Nuvasive, Inc.
6851416
In Commercial Distribution

  • 00887517379153 ()


  • Polymeric spinal interbody fusion cage
CoRoent LW, 14x11x25mm 5°
Nuvasive, Inc.
6851415
In Commercial Distribution

  • 00887517379146 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LO, 14x10x40mm 5°
Nuvasive, Inc.
6851413
In Commercial Distribution

  • 00887517379139 ()


  • Polymeric spinal interbody fusion cage
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