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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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T25 Retractor Driver
NEXUS SPINE, L.L.C.
820319.08
Not in Commercial Distribution

  • B678820319080 ()


  • Bone-screw internal spinal fixation system, sterile
Palm Ratchet
NEXUS SPINE, L.L.C.
820319.07
Not in Commercial Distribution

  • B678820319070 ()


  • Bone-screw internal spinal fixation system, sterile
Medial Rack Assy
NEXUS SPINE, L.L.C.
820319.06
Not in Commercial Distribution

  • B678820319060 ()


  • Bone-screw internal spinal fixation system, sterile
Main Frame Assy
NEXUS SPINE, L.L.C.
820319.05
Not in Commercial Distribution

  • B678820319050 ()


  • Bone-screw internal spinal fixation system, sterile
45mm Bone Anchor
NEXUS SPINE, L.L.C.
820319.04
Not in Commercial Distribution

  • B678820319040 ()

  • Length: 45 Millimeter


  • Bone-screw internal spinal fixation system, sterile
40mm Bone Anchor
NEXUS SPINE, L.L.C.
820319.03
Not in Commercial Distribution

  • B678820319030 ()

  • Length: 40 Millimeter


  • Bone-screw internal spinal fixation system, sterile
35mm Bone Anchor
NEXUS SPINE, L.L.C.
820319.02
Not in Commercial Distribution

  • B678820319020 ()

  • Length: 35 Millimeter


  • Bone-screw internal spinal fixation system, sterile
Driver, Blade/Top Interlagos
NEXUS SPINE, L.L.C.
820319.01
Not in Commercial Distribution

  • B678820319010 ()


  • Bone-screw internal spinal fixation system, sterile
MIS Interlagos Retractor
NEXUS SPINE, L.L.C.
820319
Not in Commercial Distribution

  • B6788203190 ()


  • Bone-screw internal spinal fixation system, sterile
Curved Steffee Probe – Palm Handle
NEXUS SPINE, L.L.C.
820241o
Not in Commercial Distribution

  • B67882024100 ()


  • Bone-screw internal spinal fixation system, sterile
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