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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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LIF Trial, Rasped, 8 X 22 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-08227010
In Commercial Distribution

  • 00840180511602 ()


  • Spinal implant trial
LIF Trial, Rasped, 6 X 22 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-06227010
In Commercial Distribution

  • 00840180511596 ()


  • Spinal implant trial
LIF Trial, Rasped, 4 X 22 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-04227010
In Commercial Distribution

  • 00840180511589 ()


  • Spinal implant trial
LIF Trial, Rasped, 10 X 18 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-10187010
In Commercial Distribution

  • 00840180511572 ()


  • Spinal implant trial
LIF Trial, Rasped, 8 X 18 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-08187010
In Commercial Distribution

  • 00840180511565 ()


  • Spinal implant trial
LIF Trial, Rasped, 6 X 18 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-06187010
In Commercial Distribution

  • 00840180511558 ()


  • Spinal implant trial
LIF Trial, Rasped, 4 X 18 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-04187010
In Commercial Distribution

  • 00840180511541 ()


  • Spinal implant trial
LIF Trial, 1/3 Rasped, Grooves, 12 x 22 x 70 x 10°
ALPHATEC SPINE, INC.
CI-11070-10-12227010
In Commercial Distribution

  • 00840180511251 ()


  • Spinal implant trial
LIF Trial, 1/3 Rasped, Grooves, 10 x 22 x 70 x 10°
ALPHATEC SPINE, INC.
CI-11070-10-10227010
In Commercial Distribution

  • 00840180511244 ()


  • Spinal implant trial
LIF Trial, 1/3 Rasped, Grooves, 8 x 22 x 70 x 10°
ALPHATEC SPINE, INC.
CI-11070-10-08227010
In Commercial Distribution

  • 00840180511237 ()


  • Spinal implant trial
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