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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-O Screw, 4.0x60mm 2S Uniplanar
Nuvasive, Inc.
13044060
In Commercial Distribution

  • 00887517544971 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x55mm 2S Uniplanar
Nuvasive, Inc.
13044055
In Commercial Distribution

  • 00887517544964 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x50mm 2S Uniplanar
Nuvasive, Inc.
13044050
In Commercial Distribution

  • 00887517544957 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x45mm 2S Uniplanar
Nuvasive, Inc.
13044045
In Commercial Distribution

  • 00887517544940 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x40mm 2S Uniplanar
Nuvasive, Inc.
13044040
In Commercial Distribution

  • 00887517544933 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x35mm 2S Uniplanar
Nuvasive, Inc.
13044035
In Commercial Distribution

  • 00887517544926 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x30mm 2S Uniplanar
Nuvasive, Inc.
13044030
In Commercial Distribution

  • 00887517544919 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x25mm 2S Uniplanar
Nuvasive, Inc.
13044025
In Commercial Distribution

  • 00887517544902 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x120mm 2S Uniplanar
Nuvasive, Inc.
13044012
In Commercial Distribution

  • 00887517544896 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x110mm 2S Uniplanar
Nuvasive, Inc.
13044011
In Commercial Distribution

  • 00887517544889 ()


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