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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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MIS Polyaxial Screw Driver
PRECISION SPINE, INC.
39-SP-0710
In Commercial Distribution

  • 00840019928748 ()
39-SP-0710

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Polyaxial Driver
PRECISION SPINE, INC.
39-SP-0700
In Commercial Distribution

  • 00840019928731 ()
39-SP-0700

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Dual-Side Lock Screw Driver
PRECISION SPINE, INC.
39-SP-0603
In Commercial Distribution

  • 00840019928724 ()
39-SP-0603

  • Orthopaedic surgical procedure kit, non-medicated, reusable
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
ReformĀ® Ti Reduction Driver
PRECISION SPINE, INC.
70-RT-0730
In Commercial Distribution

  • 00840019975698 ()
70-RT-0730

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

  • 00840019975674 ()
70-CT-0700

  • Orthopaedic surgical procedure kit, non-medicated, reusable
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