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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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SINGLE SLOT/CRUCIATE REPLACEMENT BLADE
Smith & Nephew, Inc.
110278
In Commercial Distribution

  • 03596010034649 ()
110278

  • Surgical screwdriver, reusable
SINGLE SL-PLUS SC-DRIVER XLGE
Smith & Nephew, Inc.
110267
In Commercial Distribution

  • 03596010034595 ()
110267

  • Surgical screwdriver, reusable
CRUCIATE SECREWDRIVER 203.2MM
Smith & Nephew, Inc.
110266
In Commercial Distribution

  • 03596010034588 ()
110266

  • Surgical screwdriver, reusable
SINGLE SLOT SCREWDRIVER 6.3MM X 260.3MM
Smith & Nephew, Inc.
110265
In Commercial Distribution

  • 03596010034571 ()
110265

  • Surgical screwdriver, reusable
6.5MM CANNULATED SCREWDRIVER WITH COUNTERSINK
Smith & Nephew, Inc.
110120
In Commercial Distribution

  • 03596010033970 ()
110120

  • 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
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