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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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LOCATOR® DRIVER TORQUE WRENCH 29MM LATCH
Zest Anchors, LLC
08914
In Commercial Distribution

  • 00893202000752 ()

  • Length: 29 Millimeter


  • Surgical screwdriver, reusable
LOCATOR® DRIVER TORQUE WRENCH 23MM LATCH
Zest Anchors, LLC
08913
In Commercial Distribution

  • 00893202000745 ()

  • Length: 23 Millimeter


  • Surgical screwdriver, reusable
LOCATOR® DRIVER FOR RATCHET, L 21.0 MM
Zest Anchors, LLC
08396
In Commercial Distribution

  • 00893202000431 ()

  • Length: 21 Millimeter


  • Surgical screwdriver, reusable
LOCATOR® DRIVER FOR RATCHET, L 15.0 MM
Zest Anchors, LLC
08395
In Commercial Distribution

  • 00893202000127 ()

  • Length: 15 Millimeter


  • Surgical screwdriver, reusable
Reduction Driver, Cannulated
PRECISION SPINE, INC.
39-SP-1770
In Commercial Distribution

  • 00840019975667 ()
39-SP-1770

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reduction Driver
PRECISION SPINE, INC.
39-SP-0770
In Commercial Distribution

  • 00840019975650 ()
39-SP-0770

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0105
In Commercial Distribution

  • 00840019973076 ()
73-BK-0105

  • Neurosurgical retraction system, spinal
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0104
In Commercial Distribution

  • 00840019973069 ()
73-BK-0104

  • Neurosurgical retraction system, spinal
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0103
In Commercial Distribution

  • 00840019973052 ()
73-BK-0103

  • Neurosurgical retraction system, spinal
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0102
In Commercial Distribution

  • 00840019973045 ()
73-BK-0102

  • Spinal bone screw, non-bioabsorbable
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