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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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BASE Trial Rasp, 10x42x36mm 10°
Nuvasive, Inc.
6957044
In Commercial Distribution

  • 00887517836663 ()


  • Spinal implant trial
BASE Trial Rasp, 8x42x36mm 10°
Nuvasive, Inc.
6957043
In Commercial Distribution

  • 00887517836656 ()


  • Spinal implant trial
BASE Trial Rasp, 6x42x36mm 10°
Nuvasive, Inc.
6957042
In Commercial Distribution

  • 00887517836649 ()


  • Spinal implant trial
BASE Trial Rasp, 4x42x36mm 10°
Nuvasive, Inc.
6957041
In Commercial Distribution

  • 00887517836632 ()


  • Spinal implant trial
BONE FILE # 10 PLAIN SERRATED
TELEFLEX INCORPORATED
IPN015674
In Commercial Distribution

  • 24026704291568 ()
  • 04026704291564 ()

  • Double ended Plain serrations
  • Length: 17.8 Centimeter
KM69542

  • Bone file/rasp, manual, reusable
BALL PROBE 10 MM ONYX
Orthofix US LLC
70-1402
In Commercial Distribution

  • 18257200065943 ()


  • Growth-correction orthopaedic fixation plate kit
CoRoent® LO, 12x10x35mm 10°
Nuvasive, Inc.
1552257
In Commercial Distribution

  • 00887517101594 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LO, 10x10x35mm 10°
Nuvasive, Inc.
1552256
In Commercial Distribution

  • 00887517101587 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LO, 8x10x35mm 10°
Nuvasive, Inc.
1552255
In Commercial Distribution

  • 00887517101570 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LO, 12x10x30mm 10°
Nuvasive, Inc.
1552253
In Commercial Distribution

  • 00887517101563 ()


  • Polymeric spinal interbody fusion cage
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