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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, 12x26x55mm 10°
Nuvasive, Inc.
8261255P2
In Commercial Distribution

  • 00887517983800 ()


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

  • 00887517983763 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 10x26x60mm 10°
Nuvasive, Inc.
8261060P2
In Commercial Distribution

  • 00887517983749 ()


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

  • 00887517983725 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 10x26x50mm 10°
Nuvasive, Inc.
8261050P2
In Commercial Distribution

  • 00887517983701 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 10x26x45mm 10°
Nuvasive, Inc.
8261045P2
In Commercial Distribution

  • 00887517983688 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 8x26x60mm 10°
Nuvasive, Inc.
8260860P2
In Commercial Distribution

  • 00887517983664 ()


  • Polymeric spinal interbody fusion cage
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
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