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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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MODIFIED LONG HEXDRIVER
Smith & Nephew, Inc.
E0017338-3
In Commercial Distribution

  • 00885556805930 ()
E0017338-3

  • Medullary canal orthopaedic reamer, rigid
MODIFIED MEDIUM HEXDRIVER
Smith & Nephew, Inc.
E0017338-2
In Commercial Distribution

  • 00885556805923 ()
E0017338-2

  • Medullary canal orthopaedic reamer, rigid
MODIFIED SHORT HEXDRIVER
Smith & Nephew, Inc.
E0017338-1
In Commercial Distribution

  • 00885556805916 ()
E0017338-1

  • Medullary canal orthopaedic reamer, rigid
BIOSURE DRIVER REFURBISHED
Smith & Nephew, Inc.
72201887F
In Commercial Distribution

  • 00885556572726 ()
72201887F

  • Surgical screwdriver, reusable
REFURBDRIVERSCR2.0MM CANN. W/3.5
Smith & Nephew, Inc.
7207268D
Not in Commercial Distribution

  • 00885556568804 ()
7207268D

  • Orthopaedic implant driver
REFURB.SLK 1.5 SCR.DRVR
Smith & Nephew, Inc.
014815D
Not in Commercial Distribution

  • 00885556558973 ()
014815D

  • Orthopaedic implant driver
MODIFIED LONG HEXDRIVER
Smith & Nephew, Inc.
E0017952-3
In Commercial Distribution

  • 00885556891209 ()
E0017952-3

  • Medullary canal orthopaedic reamer, rigid
MODIFIED MEDIUM HEXDRIVER
Smith & Nephew, Inc.
E0017952-2
In Commercial Distribution

  • 00885556891193 ()
E0017952-2

  • Medullary canal orthopaedic reamer, rigid
MODIFIED SHORT HEXDRIVER
Smith & Nephew, Inc.
E0017952-1
In Commercial Distribution

  • 00885556891186 ()
E0017952-1

  • Medullary canal orthopaedic reamer, rigid
POSTERIOR APPROACH STEM PUSHER
Smith & Nephew, Inc.
E0015433-1
In Commercial Distribution

  • 00885556689677 ()
E0015433-1

  • Orthopaedic inorganic implant inserter/extractor, reusable
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