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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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RELINE Screw, 7.0x80mm 2FC Polyaxial
Nuvasive, Inc.
16217080
In Commercial Distribution

  • 00887517924117 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 7.0x75mm 2FC Polyaxial
Nuvasive, Inc.
16217075
In Commercial Distribution

  • 00887517924100 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 7.0x70mm 2FC Polyaxial
Nuvasive, Inc.
16217070
In Commercial Distribution

  • 00887517924094 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 7.0x65mm 2FC Polyaxial
Nuvasive, Inc.
16217065
In Commercial Distribution

  • 00887517924087 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 7.0x60mm 2FC Polyaxial
Nuvasive, Inc.
16217060
In Commercial Distribution

  • 00887517924070 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 7.0x55mm 2FC Polyaxial
Nuvasive, Inc.
16217055
In Commercial Distribution

  • 00887517924063 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 7.0x50mm 2FC Polyaxial
Nuvasive, Inc.
16217050
In Commercial Distribution

  • 00887517924056 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 6.0x55mm 2FC Polyaxial
Nuvasive, Inc.
16216055
In Commercial Distribution

  • 00887517923721 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 6.0x50mm 2FC Polyaxial
Nuvasive, Inc.
16216050
In Commercial Distribution

  • 00887517923714 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 6.0x45mm 2FC Polyaxial
Nuvasive, Inc.
16216045
In Commercial Distribution

  • 00887517923707 ()


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