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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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90210 Single Use #10 Safety Scalpel
XODUS MEDICAL, INC.
90210
In Commercial Distribution

  • 10787551012108 ()
  • 00787551012101 ()
  • 20787551012105 ()
90210

  • Scalpel, single-use
XLP Lateral Plate, 2-Hole Size 10
Nuvasive, Inc.
7522010
In Commercial Distribution

  • 00887517489333 ()


  • Spinal fixation plate, non-bioabsorbable
XLP Lateral Plate, 2-Hole Size 10
Nuvasive, Inc.
7521010
In Commercial Distribution

  • 00887517489012 ()


  • Spinal fixation plate, non-bioabsorbable
Universal Guide, Size 10 Bone Mill
Nuvasive, Inc.
7510110
In Commercial Distribution

  • 00887517488671 ()


  • Surgical instrument/implant depth limiter, reusable
10.5 H x 10 W TRIAL
Orthofix US LLC
28-1010
In Commercial Distribution

  • 18257200126279 ()


  • Metallic spinal interbody fusion cage
8.5 H x 10 W TRIAL
Orthofix US LLC
28-1008
In Commercial Distribution

  • 18257200126262 ()


  • Metallic spinal interbody fusion cage
Procera Esthetic Abutment BmkSyst RP #10
Nobel Biocare AB
33763
Not in Commercial Distribution

  • 07332747002249 ()
33763

  • Dental implant suprastructure, permanent, preformed
Procera Esthetic Abutment NobRpl RP # 10
Nobel Biocare AB
33783
Not in Commercial Distribution

  • 07332747002041 ()
33783

  • Dental implant suprastructure, permanent, preformed
1.1 K-Wire, Lancet, 100mm, 10/Pkg
Medartis AG
A-5042.10
In Commercial Distribution

  • 07630008434960 ()
  • 07630037800866 ()
A-5042.10

  • Orthopaedic bone wire
0.8 K-Wire, Lancet, 100mm, 10/Pkg
Medartis AG
A-5042.00
In Commercial Distribution

  • 07630008434946 ()
  • 07630037800859 ()
A-5042.00

  • Orthopaedic bone wire
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