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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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ARM15S Screw, 7.5x50mm Fixed
Nuvasive, Inc.
8957550
In Commercial Distribution

  • 00887517393654 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 7.5x45mm Fixed
Nuvasive, Inc.
8957545
In Commercial Distribution

  • 00887517393647 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 7.5x35mm Fixed
Nuvasive, Inc.
8957535
In Commercial Distribution

  • 00887517393623 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 4.5x40mm Polyaxial TL
Nuvasive, Inc.
8834540B
In Commercial Distribution

  • 00887517393494 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 4.5x35mm Polyaxial TL
Nuvasive, Inc.
8834535A
In Commercial Distribution

  • 00887517393463 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 4.5x30mm Polyaxial TL
Nuvasive, Inc.
8834530A
In Commercial Distribution

  • 00887517393449 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 4.5x25mm Polyaxial TL
Nuvasive, Inc.
8834525B
In Commercial Distribution

  • 00887517393432 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 4.5x25mm Polyaxial TL
Nuvasive, Inc.
8834525A
In Commercial Distribution

  • 00887517393425 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 10.5x80mm Polyaxial TL
Nuvasive, Inc.
8830580A
In Commercial Distribution

  • 00887517393401 ()


  • Bone-screw internal spinal fixation system, non-sterile
CoRoent® XL Wide, 10x22x45mm Lordotic
Nuvasive, Inc.
6921045
In Commercial Distribution

  • 00887517393388 ()


  • Polymeric spinal interbody fusion cage
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