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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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ZEUS®-L, Lateral Lumber Interbody Fusion Device, 21mm x 50mm x 10mm, 14 degree Lordosis
SPINAL ELEMENTS
62-102150-14
In Commercial Distribution

  • 00840916134136 ()


  • Polymeric spinal interbody fusion cage
ZEUS®-L, Lateral Lumber Interbody Fusion Device, 21mm x 50mm x 8mm, 7 degree Lordosis
SPINAL ELEMENTS
62-182150-07
In Commercial Distribution

  • 00840916134129 ()


  • Polymeric spinal interbody fusion cage
ZEUS®-L, Lateral Lumber Interbody Fusion Device, 21mm x 50mm x 16mm, 7 degree Lordosis
SPINAL ELEMENTS
62-162150-07
In Commercial Distribution

  • 00840916134112 ()


  • Polymeric spinal interbody fusion cage
ZEUS®-L, Lateral Lumber Interbody Fusion Device, 21mm x 50mm x 12mm, 7 degree Lordosis
SPINAL ELEMENTS
62-122150-07
In Commercial Distribution

  • 00840916134099 ()


  • Polymeric spinal interbody fusion cage
ZEUS®-L, Lateral Lumber Interbody Fusion Device, 21mm x 50mm x 10mm, 7 degree Lordosis
SPINAL ELEMENTS
62-102150-07
In Commercial Distribution

  • 00840916134082 ()


  • Polymeric spinal interbody fusion cage
ZEUS®-L, Lateral Lumber Interbody Fusion Device, 21mm x 50mm x 8mm, 7 degree Lordosis
SPINAL ELEMENTS
62-082150-07
In Commercial Distribution

  • 00840916134075 ()


  • Polymeric spinal interbody fusion cage
No Description
Life Spine, Inc.
85-1555-716X
In Commercial Distribution

  • 00190837019273 ()


  • Polymeric spinal interbody fusion cage
No Description
Life Spine, Inc.
85-1555-714X
In Commercial Distribution

  • 00190837019266 ()


  • Polymeric spinal interbody fusion cage
No Description
Life Spine, Inc.
85-1555-712X
In Commercial Distribution

  • 00190837019259 ()


  • Polymeric spinal interbody fusion cage
No Description
Life Spine, Inc.
85-1555-710X
In Commercial Distribution

  • 00190837019242 ()


  • Polymeric spinal interbody fusion cage
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