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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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Poly Screw Driver
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809319787983 ()
FX.IN.0020S

  • Bone-screw internal spinal fixation system, non-sterile
Rigid Driver Shaft, CREO Fenestrated
GLOBUS MEDICAL, INC.
6192.0050
In Commercial Distribution

  • 00889095603132 ()


  • Trans-facet-screw internal spinal fixation system, sterile
Cannulated Driver Shaft, CREO Fenestrated
GLOBUS MEDICAL, INC.
6192.0040
In Commercial Distribution

  • 00889095603125 ()


  • Trans-facet-screw internal spinal fixation system, sterile
MODULAR SCREW DRIVER
Orthofix US LLC
36-1838
In Commercial Distribution

  • 18257200130290 ()


  • Bone-screw internal spinal fixation system, non-sterile
SET SCREW DRIVER
Orthofix US LLC
79-1006
In Commercial Distribution

  • 18257200125302 ()


  • Bone-screw internal spinal fixation system, non-sterile
SET SCREW INSERTER
Orthofix US LLC
79-1005
In Commercial Distribution

  • 18257200125296 ()


  • Bone-screw internal spinal fixation system, non-sterile
SET SCREW DRIVER
Orthofix US LLC
36-1161
In Commercial Distribution

  • 18257200121038 ()


  • Bone-screw internal spinal fixation system, non-sterile
MODULAR SCREW DRIVER
Orthofix US LLC
36-1836
In Commercial Distribution

  • 18257200119851 ()


  • Bone-screw internal spinal fixation system, non-sterile
MULTI-AXIAL SCREW DRIVER
Orthofix US LLC
36-1835
In Commercial Distribution

  • 18257200119844 ()


  • Bone-screw internal spinal fixation system, non-sterile
MIDLINE SCREW DRIVER
Orthofix US LLC
36-1834
In Commercial Distribution

  • 18257200119721 ()


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