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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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Trial Head 12x15x9 0 deg.
ELEVATION SPINE, INC.
CI-TH2509
In Commercial Distribution

  • 00810017912544 ()
CI-TH2509

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x8 9 deg.
ELEVATION SPINE, INC.
CI-TH2598
In Commercial Distribution

  • 00810017912650 ()
CI-TH2598

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x8 6 deg.
ELEVATION SPINE, INC.
CI-TH2568
In Commercial Distribution

  • 00810017912599 ()
CI-TH2568

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x8 0 deg.
ELEVATION SPINE, INC.
CI-TH2508
In Commercial Distribution

  • 00810017912537 ()
CI-TH2508

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x7 9 deg.
ELEVATION SPINE, INC.
CI-TH2597
In Commercial Distribution

  • 00810017912643 ()
CI-TH2597

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x7 6 deg.
ELEVATION SPINE, INC.
CI-TH2567
In Commercial Distribution

  • 00810017912582 ()
CI-TH2567

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x7 0 deg.
ELEVATION SPINE, INC.
CI-TH2507
In Commercial Distribution

  • 00810017912520 ()
CI-TH2507

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x6 9 deg.
ELEVATION SPINE, INC.
CI-TH2596
In Commercial Distribution

  • 00810017912636 ()
CI-TH2596

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x6 6 deg.
ELEVATION SPINE, INC.
CI-TH2566
In Commercial Distribution

  • 00810017912575 ()
CI-TH2566

  • Intervertebral-body internal spinal fixation system
Trial Head 12x15x6 0 deg.
ELEVATION SPINE, INC.
CI-TH2506
In Commercial Distribution

  • 00810017912513 ()
CI-TH2506

  • Intervertebral-body internal spinal fixation system
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