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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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SKLARSAFE SCALPEL #10 BNS 500
SKLAR CORPORATION
06-3130
In Commercial Distribution

  • 40649111185299 ()
  • 00649111185291 ()


  • Scalpel, single-use
CoRoent LO Ti, 12x10x40mm 10°
Nuvasive, Inc.
6091240P2
In Commercial Distribution

  • 00887517993199 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 12x10x35mm 10°
Nuvasive, Inc.
6091235P2
In Commercial Distribution

  • 00887517993182 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 12x10x30mm 10°
Nuvasive, Inc.
6091230P2
In Commercial Distribution

  • 00887517993175 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 12x10x25mm 10°
Nuvasive, Inc.
6091225P2
In Commercial Distribution

  • 00887517993168 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 11x10x40mm 10°
Nuvasive, Inc.
6091140P2
In Commercial Distribution

  • 00887517993151 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 11x10x35mm 10°
Nuvasive, Inc.
6091135P2
In Commercial Distribution

  • 00887517993144 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 11x10x30mm 10°
Nuvasive, Inc.
6091130P2
In Commercial Distribution

  • 00887517993137 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 11x10x25mm 10°
Nuvasive, Inc.
6091125P2
In Commercial Distribution

  • 00887517993120 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 10x10x40mm 10°
Nuvasive, Inc.
6091040P2
In Commercial Distribution

  • 00887517993113 ()


  • Metallic spinal interbody fusion cage
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