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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 Class Implantable

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GSB Ti Rod, 5.0x240mm Straight
Nuvasive, Inc.
15150240
In Commercial Distribution

  • 00887517292452 ()


  • Bone-screw internal spinal fixation system, non-sterile
GSB Ti Rod, 5.0x230mm Straight
Nuvasive, Inc.
15150230
In Commercial Distribution

  • 00887517292445 ()


  • Bone-screw internal spinal fixation system, non-sterile
GSB Ti Rod, 5.0x220mm Straight
Nuvasive, Inc.
15150220
In Commercial Distribution

  • 00887517292438 ()


  • Bone-screw internal spinal fixation system, non-sterile
GSB Ti Rod, 5.0x210mm Straight
Nuvasive, Inc.
15150210
In Commercial Distribution

  • 00887517292421 ()


  • Bone-screw internal spinal fixation system, non-sterile
GSB CpTi Rod, 6.0x590mm Straight
Nuvasive, Inc.
15060590
In Commercial Distribution

  • 00887517292414 ()


  • Bone-screw internal spinal fixation system, non-sterile
GSB CpTi Rod, 6.0x580mm Straight
Nuvasive, Inc.
15060580
In Commercial Distribution

  • 00887517292407 ()


  • Bone-screw internal spinal fixation system, non-sterile
CoRoent® XLFW, 14x22x60mm
Nuvasive, Inc.
6161460
In Commercial Distribution

  • 00887517292391 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLFW, 14x22x55mm
Nuvasive, Inc.
6161455
In Commercial Distribution

  • 00887517292384 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLFW, 14x22x50mm
Nuvasive, Inc.
6161450
In Commercial Distribution

  • 00887517292377 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLFW, 12x22x60mm
Nuvasive, Inc.
6161260
In Commercial Distribution

  • 00887517292353 ()


  • Polymeric spinal interbody fusion cage
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