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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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ZIMMER SPINE, INC.
3558-1
In Commercial Distribution

  • 00889024336377 ()
3558-1

  • Surgical screwdriver, reusable
SQUARE CONNECT DRIVER SHAFT, T-LIFT
SPINEFRONTIER, INC.
14-05000
In Commercial Distribution

  • 00190361023739 ()


  • Polymeric spinal interbody fusion cage
DRIVER, GEN II INSERTER, SACROFUSE
SPINEFRONTIER, INC.
14-42003
In Commercial Distribution

  • 00190361023647 ()

  • Outer Diameter: 8 Millimeter


  • Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated
IMPACT SHAFT-DRIVER, INSERTER, SACROFUSE
SPINEFRONTIER, INC.
14-42001
In Commercial Distribution

  • 00190361023272 ()


  • Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated
RETENTION SHAFT, INSERTER, SACROFUSE
SPINEFRONTIER, INC.
14-42000
In Commercial Distribution

  • 00190361023265 ()


  • Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated
SQUARE CONNECT DRIVER SHAFT, T-LIFT, 14 DEG
SPINEFRONTIER, INC.
14-05005
In Commercial Distribution

  • 00190361023210 ()


  • Polymeric spinal interbody fusion cage
DRIVER SILK SCREW 1.5MM
Smith & Nephew, Inc.
014815
In Commercial Distribution

  • 03596010026477 ()
014815

  • Orthopaedic implant driver
DRVR FIXATION POST W/HLDR.
Smith & Nephew, Inc.
013124
In Commercial Distribution

  • 03596010024664 ()
013124

  • Orthopaedic implant driver
Polyaxial Driver
PRECISION SPINE, INC.
39-SP-0720
In Commercial Distribution

  • 00840019929172 ()
39-SP-0720

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Retention Bone-Screw Driver
PRECISION SPINE, INC.
39-SP-0610
In Commercial Distribution

  • 00840019929165 ()
39-SP-0610

  • Orthopaedic surgical procedure kit, non-medicated, reusable
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