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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, 8x26x55mm 10°
Nuvasive, Inc.
8260855P2
In Commercial Distribution

  • 00887517983640 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 8x26x50mm 10°
Nuvasive, Inc.
8260850P2
In Commercial Distribution

  • 00887517983626 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 8x26x45mm 10°
Nuvasive, Inc.
8260845P2
In Commercial Distribution

  • 00887517983602 ()


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

  • 00887517983343 ()


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

  • 00887517983329 ()


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

  • 00887517983305 ()


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

  • 00887517983282 ()


  • 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
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