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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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DRIVER CANNULATED 2MM
Smith & Nephew, Inc.
7207193
In Commercial Distribution

  • 03596010253491 ()
7207193

  • Orthopaedic implant driver
Reform® Ti Locking Polyaxial Driver
PRECISION SPINE, INC.
75-RT-0700
In Commercial Distribution

  • 00840019975711 ()
75-RT-0700

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reform® Ti Reduction Driver, Cannulated
PRECISION SPINE, INC.
70-RT-1730
In Commercial Distribution

  • 00840019975704 ()
70-RT-1730

  • 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-0103
In Commercial Distribution

  • 00840019973052 ()
73-BK-0103

  • Neurosurgical retraction system, spinal
Modular T25 Driver
PRECISION SPINE, INC.
73-MD-2800
In Commercial Distribution

  • 00840019972901 ()
73-MD-2800

  • Neurosurgical retraction system, spinal
Polyaxial Driver, Cannulated
PRECISION SPINE, INC.
70-CT-1700
In Commercial Distribution

  • 00840019970976 ()
70-CT-1700

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Modular Driver, Reform Ti, Cannulated
PRECISION SPINE, INC.
75-RT-1800
In Commercial Distribution

  • 00840019970754 ()
75-RT-1800

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Locking Polyaxial Driver, Reform Ti, Cannulated
PRECISION SPINE, INC.
75-RT-1700
In Commercial Distribution

  • 00840019970730 ()
75-RT-1700

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Modular Screw Driver
PRECISION SPINE, INC.
70-MC-0820
In Commercial Distribution

  • 00840019970662 ()
70-MC-0820

  • Orthopaedic surgical procedure kit, non-medicated, reusable
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