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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 Class Implantable

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RSS Ti Rod, 4.5x55mm Straight
Nuvasive, Inc.
20345055
In Commercial Distribution

  • 00887517802330 ()


  • Bone-screw internal spinal fixation system, non-sterile
RSS Ti Rod, 4.5x50mm Straight
Nuvasive, Inc.
20345050
In Commercial Distribution

  • 00887517802323 ()


  • Bone-screw internal spinal fixation system, non-sterile
RSS Ti Rod, 4.5x45mm Straight
Nuvasive, Inc.
20345045
In Commercial Distribution

  • 00887517802316 ()


  • Bone-screw internal spinal fixation system, non-sterile
RSS Ti Rod, 4.5x40mm Straight
Nuvasive, Inc.
20345040
In Commercial Distribution

  • 00887517802309 ()


  • Bone-screw internal spinal fixation system, non-sterile
RSS Ti Rod, 4.5x35mm Straight
Nuvasive, Inc.
20345035
In Commercial Distribution

  • 00887517802293 ()


  • Bone-screw internal spinal fixation system, non-sterile
RSS Ti Rod, 4.5x30mm Straight
Nuvasive, Inc.
20345030
In Commercial Distribution

  • 00887517802286 ()


  • Bone-screw internal spinal fixation system, non-sterile
RSS Ti Rod, 4.5x25mm Straight
Nuvasive, Inc.
20345025
In Commercial Distribution

  • 00887517802279 ()


  • Bone-screw internal spinal fixation system, non-sterile
RSS Ti Rod, 4.5x20mm Straight
Nuvasive, Inc.
20345020
In Commercial Distribution

  • 00887517802262 ()


  • Bone-screw internal spinal fixation system, non-sterile
RSS Ti Rod, 4.5x15mm Straight
Nuvasive, Inc.
20345015
In Commercial Distribution

  • 00887517802255 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Silencer Removal Tool
Nuvasive, Inc.
11010740
In Commercial Distribution

  • 00887517802248 ()


  • Orthopaedic implant/instrument dismantling device
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