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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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COHERE XLXW, 12x26x50mm 10°
Nuvasive, Inc.
8261250P2
In Commercial Distribution

  • 00887517983787 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 12x26x45mm 10°
Nuvasive, Inc.
8261245P2
In Commercial Distribution

  • 00887517983763 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 10x26x55mm 10°
Nuvasive, Inc.
8261055P2
In Commercial Distribution

  • 00887517983725 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 12x22x60mm 10°
Nuvasive, Inc.
8221260P2
In Commercial Distribution

  • 00887517983343 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 12x22x50mm 10°
Nuvasive, Inc.
8221250P2
In Commercial Distribution

  • 00887517983305 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x60mm 10°
Nuvasive, Inc.
8221060P2
In Commercial Distribution

  • 00887517983268 ()


  • 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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