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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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Titanium Straight Rod 5.50 x 80mm
SPINECRAFT, LLC
SC-5500-080
In Commercial Distribution

  • M824SC55000801 ()


  • Bone-screw internal spinal fixation system
Titanium Lordosed Rod 5.50 x 70mm
SPINECRAFT, LLC
SC-5500-070L
In Commercial Distribution

  • M824SC5500070L1 ()


  • Bone-screw internal spinal fixation system
Titanium Straight Rod 5.50 x 70mm
SPINECRAFT, LLC
SC-5500-070
In Commercial Distribution

  • M824SC55000701 ()


  • Bone-screw internal spinal fixation system
Titanium Lordosed Rod 5.50 x 60mm
SPINECRAFT, LLC
SC-5500-060L
In Commercial Distribution

  • M824SC5500060L1 ()


  • Bone-screw internal spinal fixation system
Titanium Straight Rod 5.50 x 60mm
SPINECRAFT, LLC
SC-5500-060
In Commercial Distribution

  • M824SC55000601 ()


  • Bone-screw internal spinal fixation system
Titanium Lordosed Rod 5.50 x 50mm
SPINECRAFT, LLC
SC-5500-050L
In Commercial Distribution

  • M824SC5500050L1 ()


  • Bone-screw internal spinal fixation system
Titanium Lordosed Rod 5.50 x 45mm
SPINECRAFT, LLC
SC-5500-045L
In Commercial Distribution

  • M824SC5500045L1 ()


  • Bone-screw internal spinal fixation system
Titanium Lordosed Rod 5.50 x 40mm
SPINECRAFT, LLC
SC-5500-040L
In Commercial Distribution

  • M824SC5500040L1 ()


  • Bone-screw internal spinal fixation system
Titanium Lordosed Rod 5.50 x 30mm
SPINECRAFT, LLC
SC-5500-030L
In Commercial Distribution

  • M824SC5500030L1 ()


  • Bone-screw internal spinal fixation system
Titanium Straight Rod 5.50 x 30mm
SPINECRAFT, LLC
SC-5500-030
In Commercial Distribution

  • M824SC55000301 ()


  • Bone-screw internal spinal fixation system
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