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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, 4.0x50mm 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, 4.0x35mm 2S Monoaxial
Nuvasive, Inc.
13084035
In Commercial Distribution

  • 00887517549594 ()


  • 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, 12.5x90mm 2S Monoaxial
Nuvasive, Inc.
13082590
In Commercial Distribution

  • 00887517549525 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x80mm 2S Monoaxial
Nuvasive, Inc.
13082580
In Commercial Distribution

  • 00887517549501 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x75mm 2S Monoaxial
Nuvasive, Inc.
13082575
In Commercial Distribution

  • 00887517549495 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x60mm 2S Monoaxial
Nuvasive, Inc.
13082560
In Commercial Distribution

  • 00887517549464 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x50mm 2S Monoaxial
Nuvasive, Inc.
13082550
In Commercial Distribution

  • 00887517549440 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x35mm 2S Monoaxial
Nuvasive, Inc.
13082535
In Commercial Distribution

  • 00887517549419 ()


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