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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 XL+ Wide, 8x22x60mm 10°
Nuvasive, Inc.
6308260P
In Commercial Distribution

  • 00887517228611 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+ Wide, 8x22x55mm 10°
Nuvasive, Inc.
6308255P
In Commercial Distribution

  • 00887517228222 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+ Wide, 8x22x50mm 10°
Nuvasive, Inc.
6308250P
In Commercial Distribution

  • 00887517227737 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+ Wide, 8x22x45mm 10°
Nuvasive, Inc.
6308245P
In Commercial Distribution

  • 00887517227348 ()


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

  • 00887517225238 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x60mm 10°
Nuvasive, Inc.
6308860P
In Commercial Distribution

  • 00887517225214 ()


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

  • 00887517225047 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x55mm 10°
Nuvasive, Inc.
6308855P
In Commercial Distribution

  • 00887517225023 ()


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

  • 00887517224651 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x50mm 10°
Nuvasive, Inc.
6308850P
In Commercial Distribution

  • 00887517224637 ()


  • Polymeric spinal interbody fusion cage
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