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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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Cambria Rasp, 15 x 13 x 11mm, w/Depth Stop
Seaspine Orthopedics Corporation
93-9741
In Commercial Distribution

  • 10889981093617 ()

  • 15 x 13 x 11mm
93-9741

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
406997
In Commercial Distribution

  • 00880304367029 ()
406997

  • Orthopaedic inorganic implant inserter/extractor, reusable
Cambria Rasp, 15 x 13 x 9mm, w/Depth Stop
Seaspine Orthopedics Corporation
93-9739
In Commercial Distribution

  • 10889981093594 ()

  • 15 x 13 x 9mm
93-9739

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
406845
In Commercial Distribution

  • 00880304366961 ()
406845

  • Surgical drill guide, reusable
Cambria Rasp, 15 x 13 x 7mm, w/Depth Stop
Seaspine Orthopedics Corporation
93-9737
In Commercial Distribution

  • 10889981093570 ()

  • 15 x 13 x 7mm
93-9737

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
406843
In Commercial Distribution

  • 00880304366947 ()
406843

  • Surgical drill guide, reusable
Cambria Rasp, 15 x 13 x 5mm, w/Depth Stop
Seaspine Orthopedics Corporation
93-9735
In Commercial Distribution

  • 10889981093556 ()

  • 15 x 13 x 5mm
93-9735

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
406838
In Commercial Distribution

  • 00880304366923 ()

  • MEDIUM
406838

  • Surgical drill guide, reusable
Cambria Rasp, 15 x 13 x 11mm, w/Depth Stop, Flat
Seaspine Orthopedics Corporation
93-9731
In Commercial Distribution

  • 10889981093532 ()

  • 15 x 13 x 11mm
93-9731

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
406833
In Commercial Distribution

  • 00880304366909 ()
406833

  • Surgical drill guide, reusable
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