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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 Class Implantable

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RELINE MAS Ti Rod, 6.0x180mm Lordotic
Nuvasive, Inc.
11360180
In Commercial Distribution

  • 00887517505668 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x170mm Lordotic
Nuvasive, Inc.
11360170
In Commercial Distribution

  • 00887517505644 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x160mm Lordotic
Nuvasive, Inc.
11360160
In Commercial Distribution

  • 00887517505620 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x155mm Lordotic
Nuvasive, Inc.
11360155
In Commercial Distribution

  • 00887517505613 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x145mm Lordotic
Nuvasive, Inc.
11360145
In Commercial Distribution

  • 00887517505590 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x140mm Lordotic
Nuvasive, Inc.
11360140
In Commercial Distribution

  • 00887517505583 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x135mm Lordotic
Nuvasive, Inc.
11360135
In Commercial Distribution

  • 00887517505576 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x125mm Lordotic
Nuvasive, Inc.
11360125
In Commercial Distribution

  • 00887517505552 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x115mm Lordotic
Nuvasive, Inc.
11360115
In Commercial Distribution

  • 00887517505538 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x110mm Lordotic
Nuvasive, Inc.
11360110
In Commercial Distribution

  • 00887517505521 ()


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