SEARCH RESULTS FOR: hibcc(9450 results)

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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 Size Type Device Class Implantable

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Medial Blade, 90mm
NEXUS SPINE, L.L.C.
820319.21
Not in Commercial Distribution

  • B678820319210 ()

  • Length: 90 Millimeter


  • Bone-screw internal spinal fixation system, sterile
Medial Blade, 80mm
NEXUS SPINE, L.L.C.
820319.2
Not in Commercial Distribution

  • B67882031920 ()

  • Length: 80 Millimeter


  • Bone-screw internal spinal fixation system, sterile
Medial Blade, 70mm
NEXUS SPINE, L.L.C.
820319.19
Not in Commercial Distribution

  • B678820319190 ()

  • Length: 70 Millimeter


  • Bone-screw internal spinal fixation system, sterile
Medial Blade, 60mm
NEXUS SPINE, L.L.C.
820319.18
Not in Commercial Distribution

  • B678820319180 ()

  • Length: 60 Millimeter


  • Bone-screw internal spinal fixation system, sterile
Medial Blade, 50mm
NEXUS SPINE, L.L.C.
820319.17
Not in Commercial Distribution

  • B678820319170 ()

  • Length: 50 Millimeter


  • Bone-screw internal spinal fixation system, sterile
Blade Holder
NEXUS SPINE, L.L.C.
820319.16
Not in Commercial Distribution

  • B678820319160 ()


  • Bone-screw internal spinal fixation system, sterile
Reversible Blade
NEXUS SPINE, L.L.C.
820319.15
Not in Commercial Distribution

  • B678820319150 ()


  • Bone-screw internal spinal fixation system, sterile
Reversible Blade
NEXUS SPINE, L.L.C.
820319.14
Not in Commercial Distribution

  • B678820319140 ()


  • Bone-screw internal spinal fixation system, sterile
Reversible Blade
NEXUS SPINE, L.L.C.
820319.13
Not in Commercial Distribution

  • B678820319130 ()


  • Bone-screw internal spinal fixation system, sterile
Reversible Blade
NEXUS SPINE, L.L.C.
820319.12
Not in Commercial Distribution

  • B678820319120 ()


  • Bone-screw internal spinal fixation system, sterile
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