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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-W+, 9x22x60mm 10°
Nuvasive, Inc.
6309260P2
In Commercial Distribution

  • 00887517993236 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 9x22x50mm 10°
Nuvasive, Inc.
6309250P2
In Commercial Distribution

  • 00887517993212 ()


  • Polymeric spinal interbody fusion cage
Modulus Cervical, 10x19x16mm 10°
Nuvasive, Inc.
67940084P2
In Commercial Distribution

  • 00887517984197 ()


  • Polymeric spinal interbody fusion cage
Modulus Cervical, 10x17x14mm 10°
Nuvasive, Inc.
67940051P2
In Commercial Distribution

  • 00887517984166 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 12x22x55mm 10°
Nuvasive, Inc.
8221255P2
In Commercial Distribution

  • 00887517983329 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 12x22x45mm 10°
Nuvasive, Inc.
8221245P2
In Commercial Distribution

  • 00887517983282 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x55mm 10°
Nuvasive, Inc.
8221055P2
In Commercial Distribution

  • 00887517983244 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x50mm 10°
Nuvasive, Inc.
8221050P2
In Commercial Distribution

  • 00887517983220 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x45mm 10°
Nuvasive, Inc.
8221045P2
In Commercial Distribution

  • 00887517983206 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 8x22x60mm 10°
Nuvasive, Inc.
8220860P2
In Commercial Distribution

  • 00887517983183 ()


  • Polymeric spinal interbody fusion cage
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