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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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Modulus TLIF-O, 12x10x30mm 15°
Nuvasive, Inc.
2120305P2
In Commercial Distribution

  • 00887517882271 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 12x10x30mm 4°
Nuvasive, Inc.
2120304P2
In Commercial Distribution

  • 00887517882257 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 12x10x30mm 12°
Nuvasive, Inc.
2120302P2
In Commercial Distribution

  • 00887517882233 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 12x10x25mm 8°
Nuvasive, Inc.
2120258P2
In Commercial Distribution

  • 00887517882196 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 12x10x25mm 4°
Nuvasive, Inc.
2120254P2
In Commercial Distribution

  • 00887517882158 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 12x10x25mm 12°
Nuvasive, Inc.
2120252P2
In Commercial Distribution

  • 00887517882134 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 10x14x30mm 4°
Nuvasive, Inc.
2104304P2
In Commercial Distribution

  • 00887517881052 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 10x14x25mm 4°
Nuvasive, Inc.
2104254P2
In Commercial Distribution

  • 00887517880956 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 10x10x35mm 4°
Nuvasive, Inc.
2100354P2
In Commercial Distribution

  • 00887517880758 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 10x10x30mm 8°
Nuvasive, Inc.
2100308P2
In Commercial Distribution

  • 00887517880697 ()


  • Metallic spinal interbody fusion cage
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