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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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TLIF Disc shaver, Size 11
SPINECRAFT, LLC
7020-03-11
In Commercial Distribution

  • 00193082078439 ()
7020-03-11

  • General internal orthopaedic fixation system implantation kit
TLIF Disc shaver, Size 09
SPINECRAFT, LLC
7020-03-09
In Commercial Distribution

  • 00193082078422 ()
7020-03-09

  • General internal orthopaedic fixation system implantation kit
TLIF Disc shaver, Size 07
SPINECRAFT, LLC
7020-03-07
In Commercial Distribution

  • 00193082078415 ()
7020-03-07

  • General internal orthopaedic fixation system implantation kit
PLIF Disc shaver, Size 13
SPINECRAFT, LLC
7020-02-13
In Commercial Distribution

  • 00193082078408 ()
7020-02-13

  • General internal orthopaedic fixation system implantation kit
PLIF Disc shaver, Size 11
SPINECRAFT, LLC
7020-02-11
In Commercial Distribution

  • 00193082078385 ()
7020-02-11

  • General internal orthopaedic fixation system implantation kit
PLIF Disc shaver, Size 09
SPINECRAFT, LLC
7020-02-09
In Commercial Distribution

  • 00193082078361 ()
7020-02-09

  • General internal orthopaedic fixation system implantation kit
PLIF Disc shaver, Size 07
SPINECRAFT, LLC
7020-02-07
In Commercial Distribution

  • 00193082078354 ()
7020-02-07

  • General internal orthopaedic fixation system implantation kit
T-Handle, 1/4in square connection
SPINECRAFT, LLC
7020-01
In Commercial Distribution

  • 00193082078347 ()
7020-01

  • General internal orthopaedic fixation system implantation kit
ORIO-L Instrument Case 2
SPINECRAFT, LLC
7000-300
In Commercial Distribution

  • 00193082078330 ()
7000-300

  • General internal orthopaedic fixation system implantation kit
Optional Cages Caddy
SPINECRAFT, LLC
7000-213
In Commercial Distribution

  • 00193082078323 ()
7000-213

  • General internal orthopaedic fixation system implantation kit
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