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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 LO Ti, 9x10x35mm 10°
Nuvasive, Inc.
6090935P2
In Commercial Distribution

  • 00887517993069 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 9x10x30mm 10°
Nuvasive, Inc.
6090930P2
In Commercial Distribution

  • 00887517993052 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 9x10x25mm 10°
Nuvasive, Inc.
6090925P2
In Commercial Distribution

  • 00887517993045 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 8x10x40mm 10°
Nuvasive, Inc.
6090840P2
In Commercial Distribution

  • 00887517993038 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 8x10x35mm 10°
Nuvasive, Inc.
6090835P2
In Commercial Distribution

  • 00887517993021 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 8x10x30mm 10°
Nuvasive, Inc.
6090830P2
In Commercial Distribution

  • 00887517993014 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 8x10x25mm 10°
Nuvasive, Inc.
6090825P2
In Commercial Distribution

  • 00887517993007 ()


  • Metallic spinal interbody fusion cage
CoRoent® XL-XW, 16x26x55mm 10°
Nuvasive, Inc.
6216155
In Commercial Distribution

  • 00887517299758 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-XW, 16x26x50mm 10°
Nuvasive, Inc.
6216150
In Commercial Distribution

  • 00887517299741 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-XW, 16x26x45mm 10°
Nuvasive, Inc.
6216145
In Commercial Distribution

  • 00887517299734 ()


  • Polymeric spinal interbody fusion cage
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