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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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CoRoent® XL-Wide, 10x22x45mm 15°
Nuvasive, Inc.
7151045
In Commercial Distribution

  • 00887517231383 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW 15°, 8x22x55mm
Nuvasive, Inc.
7150855
In Commercial Distribution

  • 00887517231321 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW 15°, 8x22x50mm
Nuvasive, Inc.
7150850
In Commercial Distribution

  • 00887517231314 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-Wide, 8x22x45mm 15°
Nuvasive, Inc.
7150845
In Commercial Distribution

  • 00887517231307 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 9x18x60mm 10° Lordotic
Nuvasive, Inc.
1625267
In Commercial Distribution

  • 00887517230966 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 9x18x55mm 10° Lordotic
Nuvasive, Inc.
1625263
In Commercial Distribution

  • 00887517230928 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 9x18x50mm 10° Lordotic
Nuvasive, Inc.
1625259
In Commercial Distribution

  • 00887517230584 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 9x18x45mm 10° Lordotic
Nuvasive, Inc.
1625255
In Commercial Distribution

  • 00887517230546 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 9x18x40mm 10° Lordotic
Nuvasive, Inc.
1625251
In Commercial Distribution

  • 00887517230508 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-T, 8x16x50mm
Nuvasive, Inc.
1625012
In Commercial Distribution

  • 00887517230133 ()


  • Polymeric spinal interbody fusion cage
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