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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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Short Handled Driver
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662026220 ()
1022-2901

  • Metallic spinal interbody fusion cage
HANDLED LOCK CAM DRIVER
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025940 ()
1022-2201

  • Metallic spinal interbody fusion cage
STRAIGHT HANDLED DRIVER
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025933 ()
1022-2101

  • Metallic spinal interbody fusion cage
DRIVER TIP
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025896 ()
1022-1601

  • Metallic spinal interbody fusion cage
INST 9731132 KIT CR REF FRAME DRIVER 5PK
MEDTRONIC NAVIGATION, INC.
9731132
In Commercial Distribution

  • 00721902963513 ()
  • 70721902963512 ()


  • Multi-purpose stereotactic surgery system
Angled Driver
ELEVATION SPINE, INC.
CI-ANG-DRIVER
In Commercial Distribution

  • 00810017914159 ()
CI-ANG-DRIVER

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 10mm
ELEVATION SPINE, INC.
CI-DRIVER3-SP-10
In Commercial Distribution

  • 00810017913565 ()
CI-DRIVER3-SP-10

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 8-9mm
ELEVATION SPINE, INC.
CI-DRIVER3-SP-89
In Commercial Distribution

  • 00810017913558 ()
CI-DRIVER3-SP-89

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 5-7mm
ELEVATION SPINE, INC.
CI-DRIVER3-SP-567
In Commercial Distribution

  • 00810017913541 ()
CI-DRIVER3-SP-567

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 10mm
ELEVATION SPINE, INC.
CI-DRIVER-SP-10
In Commercial Distribution

  • 00810017913244 ()
CI-DRIVER-SP-10

  • Internal spinal fixation procedure kit, single-use
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