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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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Reduction Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
87772
In Commercial Distribution

  • 00190376002996 ()


  • Surgical screwdriver, reusable
Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
87771
In Commercial Distribution

  • 00190376002965 ()


  • Surgical screwdriver, reusable
Reduction Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
73768
In Commercial Distribution

  • 00190376002521 ()


  • Surgical screwdriver, reusable
REFLECTION DEAD BLOW MALLET
Smith & Nephew, Inc.
71362106
Not in Commercial Distribution

  • 03596010198761 ()
71362106

  • Surgical mallet
SOLID CAPTIVE HEX DRIVER REVERSE TWIST 3.5MM HEX
Smith & Nephew, Inc.
71119013
In Commercial Distribution

  • 03596010298997 ()
71119013

  • Surgical screwdriver, reusable
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 MIS Driver
PRECISION SPINE, INC.
70-CT-0750
In Commercial Distribution

  • 00840019975681 ()
70-CT-0750

  • 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, 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
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