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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, 14x18x50mm 10°
Nuvasive, Inc.
6981450
In Commercial Distribution

  • 00887517403551 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 14x18x45mm 10°
Nuvasive, Inc.
6981445
In Commercial Distribution

  • 00887517403544 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 14x18x40mm 10°
Nuvasive, Inc.
6981440
In Commercial Distribution

  • 00887517403537 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 12x18x60mm 10°
Nuvasive, Inc.
6981260
In Commercial Distribution

  • 00887517403520 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 12x18x55mm 10°
Nuvasive, Inc.
6981255
In Commercial Distribution

  • 00887517403513 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 12x18x50mm 10°
Nuvasive, Inc.
6981250
In Commercial Distribution

  • 00887517403506 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 12x18x45mm 10°
Nuvasive, Inc.
6981245
In Commercial Distribution

  • 00887517403292 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 10x18x55mm 10°
Nuvasive, Inc.
6981055
In Commercial Distribution

  • 00887517403261 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 10x18x50mm 10°
Nuvasive, Inc.
6981050
In Commercial Distribution

  • 00887517403254 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 10x18x45mm 10°
Nuvasive, Inc.
6981045
In Commercial Distribution

  • 00887517403247 ()


  • Polymeric spinal interbody fusion cage
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