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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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CoRoent® XL, 8x18x45mm
Nuvasive, Inc.
6908845P
In Commercial Distribution

  • 00887517218957 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 16x18x40mm
Nuvasive, Inc.
6916840P
In Commercial Distribution

  • 00887517218940 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 14x18x40mm
Nuvasive, Inc.
6914840P
In Commercial Distribution

  • 00887517218933 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 12x18x40mm
Nuvasive, Inc.
6912840P
In Commercial Distribution

  • 00887517218926 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 10x18x40mm
Nuvasive, Inc.
6910840P
In Commercial Distribution

  • 00887517218919 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 8x18x40mm
Nuvasive, Inc.
6908840P
In Commercial Distribution

  • 00887517218902 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 8x18x50mm 10° Bulleted
Nuvasive, Inc.
1625452
In Commercial Distribution

  • 00887517217745 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x45mm 10° Bulleted
Nuvasive, Inc.
1625451
In Commercial Distribution

  • 00887517217738 ()


  • Polymeric spinal interbody fusion cage
CoRoent® SI, 12x19x16mm 10° Ta
Nuvasive, Inc.
6790532
In Commercial Distribution

  • 00887517205810 ()


  • Polymeric spinal interbody fusion cage
CoRoent® SI, 11x19x16mm 10° Ta
Nuvasive, Inc.
6790531
In Commercial Distribution

  • 00887517205803 ()


  • Polymeric spinal interbody fusion cage
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