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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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Oblique TLIF, 8x14x35mm 12°
Nuvasive, Inc.
5384352P2
In Commercial Distribution

  • 00887517736635 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x35mm 0°
Nuvasive, Inc.
5384350P2
In Commercial Distribution

  • 00887517736628 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x30mm 8°
Nuvasive, Inc.
5384308P2
In Commercial Distribution

  • 00887517736611 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x30mm 4°
Nuvasive, Inc.
5384304P2
In Commercial Distribution

  • 00887517736604 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x30mm 12°
Nuvasive, Inc.
5384302P2
In Commercial Distribution

  • 00887517736598 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x30mm 0°
Nuvasive, Inc.
5384300P2
In Commercial Distribution

  • 00887517736581 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x25mm 8°
Nuvasive, Inc.
5384258P2
In Commercial Distribution

  • 00887517736574 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x25mm 4°
Nuvasive, Inc.
5384254P2
In Commercial Distribution

  • 00887517736567 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x25mm 12°
Nuvasive, Inc.
5384252P2
In Commercial Distribution

  • 00887517736550 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x14x25mm 0°
Nuvasive, Inc.
5384250P2
In Commercial Distribution

  • 00887517736543 ()


  • Polymeric spinal interbody fusion cage
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