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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, 8x14x30mm 0°
Nuvasive, Inc.
5384300P2
In Commercial Distribution

  • 00887517736581 ()


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

  • 00887517736543 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x40mm 0°
Nuvasive, Inc.
5380400P2
In Commercial Distribution

  • 00887517736482 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x35mm 0°
Nuvasive, Inc.
5380350P2
In Commercial Distribution

  • 00887517736444 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x30mm 0°
Nuvasive, Inc.
5380300P2
In Commercial Distribution

  • 00887517736406 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x25mm 0°
Nuvasive, Inc.
5380250P2
In Commercial Distribution

  • 00887517736369 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 7x14x40mm 0°
Nuvasive, Inc.
5374400P2
In Commercial Distribution

  • 00887517736321 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 7x14x35mm 0°
Nuvasive, Inc.
5374350P2
In Commercial Distribution

  • 00887517736284 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 7x14x30mm 0°
Nuvasive, Inc.
5374300P2
In Commercial Distribution

  • 00887517736246 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 7x14x25mm 0°
Nuvasive, Inc.
5374250P2
In Commercial Distribution

  • 00887517736208 ()


  • Polymeric spinal interbody fusion cage
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