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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, 14x10x40mm 0°
Nuvasive, Inc.
5340400P2
In Commercial Distribution

  • 00887517735003 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x35mm 0°
Nuvasive, Inc.
5340350P2
In Commercial Distribution

  • 00887517734969 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x30mm 0°
Nuvasive, Inc.
5340300P2
In Commercial Distribution

  • 00887517734921 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x25mm 0°
Nuvasive, Inc.
5340250P2
In Commercial Distribution

  • 00887517734884 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x40mm 0°
Nuvasive, Inc.
5334400P2
In Commercial Distribution

  • 00887517734846 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x35mm 0°
Nuvasive, Inc.
5334350P2
In Commercial Distribution

  • 00887517734808 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x30mm 0°
Nuvasive, Inc.
5334300P2
In Commercial Distribution

  • 00887517734761 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x25mm 0°
Nuvasive, Inc.
5334250P2
In Commercial Distribution

  • 00887517734723 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x10x40mm 0°
Nuvasive, Inc.
5330400P2
In Commercial Distribution

  • 00887517734662 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x10x35mm 0°
Nuvasive, Inc.
5330350P2
In Commercial Distribution

  • 00887517734624 ()


  • Polymeric spinal interbody fusion cage
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