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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 Lock Screw, 5.5mm Open Tulip
Nuvasive, Inc.
13550000
In Commercial Distribution

  • 00887517551702 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x95mm 2S Monoaxial
Nuvasive, Inc.
13089595
In Commercial Distribution

  • 00887517551696 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x90mm 2S Monoaxial
Nuvasive, Inc.
13089590
In Commercial Distribution

  • 00887517551689 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x85mm 2S Monoaxial
Nuvasive, Inc.
13089585
In Commercial Distribution

  • 00887517551672 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x80mm 2S Monoaxial
Nuvasive, Inc.
13089580
In Commercial Distribution

  • 00887517551665 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x75mm 2S Monoaxial
Nuvasive, Inc.
13089575
In Commercial Distribution

  • 00887517551658 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x70mm 2S Monoaxial
Nuvasive, Inc.
13089570
In Commercial Distribution

  • 00887517551641 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x65mm 2S Monoaxial
Nuvasive, Inc.
13089565
In Commercial Distribution

  • 00887517551634 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x60mm 2S Monoaxial
Nuvasive, Inc.
13089560
In Commercial Distribution

  • 00887517551627 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x55mm 2S Monoaxial
Nuvasive, Inc.
13089555
In Commercial Distribution

  • 00887517551610 ()


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