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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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RELINE-One Shank, 5.5x45mm 2FC MOD FEN
Nuvasive, Inc.
24035545
In Commercial Distribution

  • 00195377041913 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Shank, 5.5x40mm 2FC MOD FEN
Nuvasive, Inc.
24035540
In Commercial Distribution

  • 00195377041906 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Shank, 5.5x35mm 2FC MOD FEN
Nuvasive, Inc.
24035535
In Commercial Distribution

  • 00195377041890 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Screw, 7.5x55mm 2C Polyaxial
Nuvasive, Inc.
24027555
In Commercial Distribution

  • 00195377041883 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Screw, 7.5x50mm 2C Polyaxial
Nuvasive, Inc.
24027550
In Commercial Distribution

  • 00195377041876 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Screw, 7.5x45mm 2C Polyaxial
Nuvasive, Inc.
24027545
In Commercial Distribution

  • 00195377041869 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Screw, 7.5x40mm 2C Polyaxial
Nuvasive, Inc.
24027540
In Commercial Distribution

  • 00195377041852 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Screw, 7.5x35mm 2C Polyaxial
Nuvasive, Inc.
24027535
In Commercial Distribution

  • 00195377041845 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Screw, 6.5x55mm 2C Polyaxial
Nuvasive, Inc.
24026555
In Commercial Distribution

  • 00195377041838 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-One Screw, 6.5x50mm 2C Polyaxial
Nuvasive, Inc.
24026550
In Commercial Distribution

  • 00195377041821 ()


  • Bone-screw internal spinal fixation system, non-sterile
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