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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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CoRoent® XLF, 10x18x50mm 10°
Nuvasive, Inc.
7871050
In Commercial Distribution

  • 00887517160027 ()


  • Metallic spinal interbody fusion cage
CoRoent® XLF, 8x18x55mm 10°
Nuvasive, Inc.
7870855
In Commercial Distribution

  • 00887517159694 ()


  • Metallic spinal interbody fusion cage
CoRoent® XLF, 8x18x50mm 10°
Nuvasive, Inc.
7870850
In Commercial Distribution

  • 00887517159687 ()


  • Metallic spinal interbody fusion cage
CoRoent® XLF, 8x18x45mm 10°
Nuvasive, Inc.
7870845
In Commercial Distribution

  • 00887517159670 ()


  • Metallic spinal interbody fusion cage
CoRoent® XL+, 10x18x60mm 10°
Nuvasive, Inc.
6310860
In Commercial Distribution

  • 00887517306586 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x55mm 10°
Nuvasive, Inc.
6310855
In Commercial Distribution

  • 00887517306579 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x50mm 10°
Nuvasive, Inc.
6310850
In Commercial Distribution

  • 00887517306562 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x45mm 10°
Nuvasive, Inc.
6310845
In Commercial Distribution

  • 00887517306555 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x40mm 10°
Nuvasive, Inc.
6310840
In Commercial Distribution

  • 00887517306548 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 10x22x60mm 10°
Nuvasive, Inc.
6310260
In Commercial Distribution

  • 00887517306524 ()


  • Polymeric spinal interbody fusion cage
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