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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 Ti Rod, 5.5x30mm Lordotic
Nuvasive, Inc.
14355030
In Commercial Distribution

  • 00887517508164 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.5x25mm Lordotic
Nuvasive, Inc.
14355025
In Commercial Distribution

  • 00887517508157 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.5x20mm Lordotic
Nuvasive, Inc.
14355020
In Commercial Distribution

  • 00887517508140 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.5x15mm Lordotic
Nuvasive, Inc.
14355015
In Commercial Distribution

  • 00887517508133 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x200mm Lordotic
Nuvasive, Inc.
14350200
In Commercial Distribution

  • 00887517508126 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x195mm Lordotic
Nuvasive, Inc.
14350195
In Commercial Distribution

  • 00887517508119 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x190mm Lordotic
Nuvasive, Inc.
14350190
In Commercial Distribution

  • 00887517508102 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x185mm Lordotic
Nuvasive, Inc.
14350185
In Commercial Distribution

  • 00887517508096 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x180mm Lordotic
Nuvasive, Inc.
14350180
In Commercial Distribution

  • 00887517508089 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x175mm Lordotic
Nuvasive, Inc.
14350175
In Commercial Distribution

  • 00887517508072 ()


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