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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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SET SCREW DRIVER 150
Orthofix US LLC
55-1061
In Commercial Distribution

  • 18257200053858 ()


  • Bone-screw internal spinal fixation system, non-sterile
SET SCREW DRIVER/HOLDER
Orthofix US LLC
55-1060
In Commercial Distribution

  • 18257200053841 ()


  • Bone-screw internal spinal fixation system, non-sterile
LOCKING MULTI-AXIAL SCREW DRIVER
Orthofix US LLC
55-1038
In Commercial Distribution

  • 18257200053698 ()


  • Bone-screw internal spinal fixation system, non-sterile
MODULAR SCREW DRIVER, DISASSEMBLABLE
Orthofix US LLC
52-1833
In Commercial Distribution

  • 18257200047529 ()


  • Bone-screw internal spinal fixation system, non-sterile
MULTI AXIAL SCREW DRIVER
Orthofix US LLC
52-1831
In Commercial Distribution

  • 18257200047505 ()


  • Bone-screw internal spinal fixation system, non-sterile
MONO AXIAL SCREW DRIVER
Orthofix US LLC
52-1830
In Commercial Distribution

  • 18257200047499 ()


  • Bone-screw internal spinal fixation system, non-sterile
DRIVER, TUBULAR ROD REDUCER
Orthofix US LLC
51-1990
In Commercial Distribution

  • 18257200045754 ()


  • Bone-screw internal spinal fixation system, non-sterile
MULTI-AXIAL REDUCTION SCREW DRIVER
Orthofix US LLC
61-1331
In Commercial Distribution

  • 18257200059775 ()


  • Bone-screw internal spinal fixation system, non-sterile
MONO-AXIAL REDUCTION SCREW DRIVER
Orthofix US LLC
61-1330
In Commercial Distribution

  • 18257200059768 ()


  • Bone-screw internal spinal fixation system, non-sterile
MONO-AXIAL REDUCTION SCREW DRIVER
Orthofix US LLC
61-1030
In Commercial Distribution

  • 18257200059737 ()


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