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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 Class Implantable

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Interlock II, 12x17x14mm 25°
Nuvasive, Inc.
6771225
In Commercial Distribution

  • 00887517809896 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 12x17x14mm 15°
Nuvasive, Inc.
6771215
In Commercial Distribution

  • 00887517809858 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 11x17x14mm 25°
Nuvasive, Inc.
6771125
In Commercial Distribution

  • 00887517809773 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 11x17x14mm 15°
Nuvasive, Inc.
6771115
In Commercial Distribution

  • 00887517809735 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 6x17x14mm 7°
Nuvasive, Inc.
6770607
In Commercial Distribution

  • 00887517809315 ()


  • Polymeric spinal interbody fusion cage
RELINE-O Conn, 60mm Offset with Tab
Nuvasive, Inc.
11200460
In Commercial Distribution

  • 00887517804778 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Conn, 40mm Offset with Tab
Nuvasive, Inc.
11200440
In Commercial Distribution

  • 00887517804754 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Conn, 30mm Offset with Tab
Nuvasive, Inc.
11200430
In Commercial Distribution

  • 00887517804747 ()


  • Bone-screw internal spinal fixation system, non-sterile
ALBINS Endplate Scraper, 5x12mm Bayonet
Nuvasive, Inc.
6999205
In Commercial Distribution

  • 00887517804082 ()


  • External spinal fixation system
ALBINS Cobb, 22mm Swan Inferior
Nuvasive, Inc.
6996122
In Commercial Distribution

  • 00887517803771 ()


  • External spinal fixation system
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