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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-O Screw, 5.5x110mm 2S Reduction
Nuvasive, Inc.
13025511
In Commercial Distribution

  • 00887517540034 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.5x100mm 2S Reduction
Nuvasive, Inc.
13025510
In Commercial Distribution

  • 00887517540027 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x95mm 2S Reduction
Nuvasive, Inc.
13025095
In Commercial Distribution

  • 00887517540010 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x90mm 2S Reduction
Nuvasive, Inc.
13025090
In Commercial Distribution

  • 00887517540003 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x85mm 2S Reduction
Nuvasive, Inc.
13025085
In Commercial Distribution

  • 00887517539991 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x80mm 2S Reduction
Nuvasive, Inc.
13025080
In Commercial Distribution

  • 00887517539984 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x75mm 2S Reduction
Nuvasive, Inc.
13025075
In Commercial Distribution

  • 00887517539977 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x70mm 2S Reduction
Nuvasive, Inc.
13025070
In Commercial Distribution

  • 00887517539960 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x65mm 2S Reduction
Nuvasive, Inc.
13025065
In Commercial Distribution

  • 00887517539953 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x60mm 2S Reduction
Nuvasive, Inc.
13025060
In Commercial Distribution

  • 00887517539946 ()


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