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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, 6.0x85mm Lordotic
Nuvasive, Inc.
11360085
In Commercial Distribution

  • 00887517505477 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x80mm Lordotic
Nuvasive, Inc.
11360080
In Commercial Distribution

  • 00887517505460 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x75mm Lordotic
Nuvasive, Inc.
11360075
In Commercial Distribution

  • 00887517505453 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x70mm Lordotic
Nuvasive, Inc.
11360070
In Commercial Distribution

  • 00887517505446 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x65mm Lordotic
Nuvasive, Inc.
11360065
In Commercial Distribution

  • 00887517505439 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x60mm Lordotic
Nuvasive, Inc.
11360060
In Commercial Distribution

  • 00887517505422 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x55mm Lordotic
Nuvasive, Inc.
11360055
In Commercial Distribution

  • 00887517505415 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x50mm Lordotic
Nuvasive, Inc.
11360050
In Commercial Distribution

  • 00887517505408 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x45mm Lordotic
Nuvasive, Inc.
11360045
In Commercial Distribution

  • 00887517505392 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Ti Rod, 6.0x40mm Lordotic
Nuvasive, Inc.
11360040
In Commercial Distribution

  • 00887517505385 ()


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