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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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Retention Bone-Screw Driver
PRECISION SPINE, INC.
39-SP-0601
In Commercial Distribution

  • 00840019928700 ()
39-SP-0601

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Self-Retaining T20 Driver
PRECISION SPINE, INC.
39-CC-0401
In Commercial Distribution

  • 00840019928168 ()
39-CC-0401

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Adjustment Screw Driver
PRECISION SPINE, INC.
59-SP-0601
In Commercial Distribution

  • 00840019927987 ()
59-SP-0601

  • Orthopaedic surgical procedure kit, non-medicated, reusable
SOLID CAPTIVE HEX DRIVER REVERSE TWIST 3.5MM HEX
Smith & Nephew, Inc.
71119013
In Commercial Distribution

  • 03596010298997 ()
71119013

  • Surgical screwdriver, reusable
DRIVER CANNULATED 2MM
Smith & Nephew, Inc.
7207193
In Commercial Distribution

  • 03596010253491 ()
7207193

  • Orthopaedic implant driver
Reform® Ti Reduction Driver
PRECISION SPINE, INC.
70-RT-0730
In Commercial Distribution

  • 00840019975698 ()
70-RT-0730

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reform® Ti CT Polyaxial Driver
PRECISION SPINE, INC.
70-CT-0700
In Commercial Distribution

  • 00840019975674 ()
70-CT-0700

  • 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-0103
In Commercial Distribution

  • 00840019973052 ()
73-BK-0103

  • Neurosurgical retraction system, spinal
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