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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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No Description
Biomet Orthopedics, LLC
110025324
In Commercial Distribution

  • 00887868544484 ()

  • 24 MM
110025324

  • Orthopaedic bone screw, non-bioabsorbable, non-sterile
No Description
Biomet Orthopedics, LLC
32-348074
In Commercial Distribution

  • 00887868483868 ()

  • 24 mm
32-348074

  • Bone-resection orthopaedic reamer, reusable
No Description
Biomet Orthopedics, LLC
31-301835
In Commercial Distribution

  • 00887868477799 ()

  • 24 mm
31-301835

  • Medullary canal orthopaedic reamer, flexible
No Description
Biomet Orthopedics, LLC
31-300574
In Commercial Distribution

  • 00887868475351 ()

  • Size 24
31-300574

  • Bone-resection orthopaedic reamer, reusable
No Description
Biomet Orthopedics, LLC
32-488729
In Commercial Distribution

  • 00887868497506 ()

  • 24 mm
32-488729

  • Orthopaedic prosthesis implantation positioning instrument, reusable
No Description
Biomet Orthopedics, LLC
32-360894
In Commercial Distribution

  • 00887868484780 ()

  • 24 mm
32-360894

  • Medullary canal orthopaedic reamer, flexible
No Description
Biomet Orthopedics, LLC
32-481019
In Commercial Distribution

  • 00887868489020 ()

  • 24 mm
32-481019

  • Knee femur prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
32-360624
In Commercial Distribution

  • 00887868564079 ()

  • 24 mm
32-360624

  • Medullary canal orthopaedic reamer, rigid
ANDREWS PYNCHON, 2.3 MM DIAMETER
KLS-Martin L.P.
96-256-50-01
In Commercial Distribution

  • 00888118090171 ()

  • 24 CM


  • Surgical/emergency suction cannula, non-illuminating, reusable
ANDREWS PYNCHON, 2.0 MM FRONT PORT
KLS-Martin L.P.
96-256-25-01
In Commercial Distribution

  • 00888118090126 ()

  • 24 CM


  • Surgical/emergency suction cannula, non-illuminating, reusable
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