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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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Modulus TLIF-A, 10x14x34mm 15°
Nuvasive, Inc.
1104345P2
In Commercial Distribution

  • 00887517854872 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x11x34mm 8°
Nuvasive, Inc.
1101348P2
In Commercial Distribution

  • 00887517853097 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x11x34mm 15°
Nuvasive, Inc.
1101345P2
In Commercial Distribution

  • 00887517853073 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 9x9x30mm 8°
Nuvasive, Inc.
1099308P2
In Commercial Distribution

  • 00887517851697 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 9x9x30mm 15°
Nuvasive, Inc.
1099305P2
In Commercial Distribution

  • 00887517851673 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 9x14x40mm 15°
Nuvasive, Inc.
1094405P2
In Commercial Distribution

  • 00887517851475 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 9x11x30mm 8°
Nuvasive, Inc.
1091308P2
In Commercial Distribution

  • 00887517849298 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 9x11x30mm 15°
Nuvasive, Inc.
1091305P2
In Commercial Distribution

  • 00887517849274 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 9x11x30mm 12°
Nuvasive, Inc.
1091302P2
In Commercial Distribution

  • 00887517849236 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 8x9x30mm 15°
Nuvasive, Inc.
1089305P2
In Commercial Distribution

  • 00887517848079 ()


  • Metallic spinal interbody fusion cage
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