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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, 7x10x40mm 0°
Nuvasive, Inc.
5370400P2
In Commercial Distribution

  • 00887517736147 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 7x10x35mm 0°
Nuvasive, Inc.
5370350P2
In Commercial Distribution

  • 00887517736109 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 7x10x30mm 0°
Nuvasive, Inc.
5370300P2
In Commercial Distribution

  • 00887517736062 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 7x10x25mm 0°
Nuvasive, Inc.
5370250P2
In Commercial Distribution

  • 00887517736024 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 16x14x40mm 0°
Nuvasive, Inc.
5364400P2
In Commercial Distribution

  • 00887517735980 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 16x14x35mm 0°
Nuvasive, Inc.
5364350P2
In Commercial Distribution

  • 00887517735942 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 16x14x30mm 0°
Nuvasive, Inc.
5364300P2
In Commercial Distribution

  • 00887517735904 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 16x14x25mm 0°
Nuvasive, Inc.
5364250P2
In Commercial Distribution

  • 00887517735867 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 16x10x40mm 0°
Nuvasive, Inc.
5360400P2
In Commercial Distribution

  • 00887517735683 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 16x10x35mm 0°
Nuvasive, Inc.
5360350P2
In Commercial Distribution

  • 00887517735645 ()


  • Polymeric spinal interbody fusion cage
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