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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 Class Implantable

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RELINE-O Screw, 4.0x55mm 2S Monoaxial
Nuvasive, Inc.
13084055
In Commercial Distribution

  • 00887517549631 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x50mm 2S Monoaxial
Nuvasive, Inc.
13084050
In Commercial Distribution

  • 00887517549624 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x45mm 2S Monoaxial
Nuvasive, Inc.
13084045
In Commercial Distribution

  • 00887517549617 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x40mm 2S Monoaxial
Nuvasive, Inc.
13084040
In Commercial Distribution

  • 00887517549600 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x35mm 2S Monoaxial
Nuvasive, Inc.
13084035
In Commercial Distribution

  • 00887517549594 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x30mm 2S Monoaxial
Nuvasive, Inc.
13084030
In Commercial Distribution

  • 00887517549587 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x25mm 2S Monoaxial
Nuvasive, Inc.
13084025
In Commercial Distribution

  • 00887517549570 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x120mm 2S Monoaxial
Nuvasive, Inc.
13084012
In Commercial Distribution

  • 00887517549563 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x110mm 2S Monoaxial
Nuvasive, Inc.
13084011
In Commercial Distribution

  • 00887517549556 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x100mm 2S Monoaxial
Nuvasive, Inc.
13084010
In Commercial Distribution

  • 00887517549549 ()


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