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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, 4.0x35mm 2S PLS
Nuvasive, Inc.
13064035
In Commercial Distribution

  • 00887517547071 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x30mm 2S PLS
Nuvasive, Inc.
13064030
In Commercial Distribution

  • 00887517547064 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x120mm 2S PLS
Nuvasive, Inc.
13064012
In Commercial Distribution

  • 00887517547040 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x100mm 2S PLS
Nuvasive, Inc.
13064010
In Commercial Distribution

  • 00887517547026 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.5x70mm 2S Red Uni
Nuvasive, Inc.
13056570
In Commercial Distribution

  • 00887517546968 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.5x60mm 2S Red Uni
Nuvasive, Inc.
13056560
In Commercial Distribution

  • 00887517546944 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.5x45mm 2S Red Uni
Nuvasive, Inc.
13056545
In Commercial Distribution

  • 00887517546913 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x50mm 2S Red Uni
Nuvasive, Inc.
13056050
In Commercial Distribution

  • 00887517546746 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x45mm 2S Red Uni
Nuvasive, Inc.
13056045
In Commercial Distribution

  • 00887517546739 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x30mm 2S Red Uni
Nuvasive, Inc.
13056030
In Commercial Distribution

  • 00887517546708 ()


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