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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, 12x10x35mm 0°
Nuvasive, Inc.
5320350P2
In Commercial Distribution

  • 00887517734280 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x30mm 0°
Nuvasive, Inc.
5320300P2
In Commercial Distribution

  • 00887517734242 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x14x40mm 0°
Nuvasive, Inc.
5314400P2
In Commercial Distribution

  • 00887517734167 ()


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

  • 00887517733948 ()


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

  • 00887517733863 ()


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

  • 00887517733788 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x30mm 0°
Nuvasive, Inc.
5304300P2
In Commercial Distribution

  • 00887517733740 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x25mm 0°
Nuvasive, Inc.
5304250P2
In Commercial Distribution

  • 00887517733702 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x40mm 0°
Nuvasive, Inc.
5300400P2
In Commercial Distribution

  • 00887517733641 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x35mm 0°
Nuvasive, Inc.
5300350P2
In Commercial Distribution

  • 00887517733603 ()


  • Polymeric spinal interbody fusion cage
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