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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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Oblique TLIF, 10x10x35mm 4°
Nuvasive, Inc.
5300354P2
In Commercial Distribution

  • 00887517733627 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x35mm 12°
Nuvasive, Inc.
5300352P2
In Commercial Distribution

  • 00887517733610 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x35mm 0°
Nuvasive, Inc.
5300350P2
In Commercial Distribution

  • 00887517733603 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x30mm 8°
Nuvasive, Inc.
5300308P2
In Commercial Distribution

  • 00887517733597 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x30mm 12°
Nuvasive, Inc.
5300302P2
In Commercial Distribution

  • 00887517733573 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x25mm 8°
Nuvasive, Inc.
5300258P2
In Commercial Distribution

  • 00887517733559 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x25mm 0°
Nuvasive, Inc.
5300250P2
In Commercial Distribution

  • 00887517733528 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 14x11x30mm 12°
Nuvasive, Inc.
5241302P2
In Commercial Distribution

  • 00887517733313 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x9x30mm 8°
Nuvasive, Inc.
5229308P2
In Commercial Distribution

  • 00887517733290 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x14x30mm 8°
Nuvasive, Inc.
5224308P2
In Commercial Distribution

  • 00887517733269 ()


  • Polymeric spinal interbody fusion cage
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