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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 Size Type Device Class Implantable

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Oblique TLIF, 12x14x30mm 0°
Nuvasive, Inc.
5324300P2
In Commercial Distribution

  • 00887517734426 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x35mm 0°
Nuvasive, Inc.
5320350P2
In Commercial Distribution

  • 00887517734280 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x14x35mm 0°
Nuvasive, Inc.
5314350P2
In Commercial Distribution

  • 00887517734129 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x14x30mm 0°
Nuvasive, Inc.
5314300P2
In Commercial Distribution

  • 00887517734082 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x40mm 0°
Nuvasive, Inc.
5310400P2
In Commercial Distribution

  • 00887517733986 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x35mm 0°
Nuvasive, Inc.
5310350P2
In Commercial Distribution

  • 00887517733948 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x30mm 0°
Nuvasive, Inc.
5310300P2
In Commercial Distribution

  • 00887517733900 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x25mm 0°
Nuvasive, Inc.
5310250P2
In Commercial Distribution

  • 00887517733863 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x40mm 0°
Nuvasive, Inc.
5304400P2
In Commercial Distribution

  • 00887517733825 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x35mm 0°
Nuvasive, Inc.
5304350P2
In Commercial Distribution

  • 00887517733788 ()


  • Polymeric spinal interbody fusion cage
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