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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 NM Trial w/ Depth Stop, Flat 13x12, 9mm
Seaspine Orthopedics Corporation
93-9839
In Commercial Distribution

  • 10889981093884 ()

  • 13x12, 9mm
93-9839

  • Spinal implant trial
Cambria NM Trial w/ Depth Stop, Flat 13x12, 7mm
Seaspine Orthopedics Corporation
93-9837
In Commercial Distribution

  • 10889981093860 ()

  • 13x12, 7mm
93-9837

  • Spinal implant trial
Cambria NM Trial w/ Depth Stop, Flat 13x12, 5mm
Seaspine Orthopedics Corporation
93-9835
In Commercial Distribution

  • 10889981093846 ()

  • 13x12, 5mm
93-9835

  • Spinal implant trial
Cambria NM Rasp
Seaspine Orthopedics Corporation
93-9833
In Commercial Distribution

  • 10889981093822 ()
93-9833

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
408034
In Commercial Distribution

  • 00880304367876 ()
408034

  • Bone lever/elevator, reusable
Cambria Rasp, 13 x 12 x 12mm, w/Depth Stop, Flat
Seaspine Orthopedics Corporation
93-9822
In Commercial Distribution

  • 10889981093785 ()

  • 13 x 12 x 12mm
93-9822

  • Bone file/rasp, manual, reusable
Cambria Rasp, 13 x 12 x 11mm, w/Depth Stop, Flat
Seaspine Orthopedics Corporation
93-9821
In Commercial Distribution

  • 10889981093778 ()

  • 13 x 12 x 11mm
93-9821

  • Bone file/rasp, manual, reusable
Cambria Rasp, 13 x 12 x 10mm, w/Depth Stop, Flat
Seaspine Orthopedics Corporation
93-9820
In Commercial Distribution

  • 10889981093761 ()

  • 13 x 12 x 10mm
93-9820

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
407015
In Commercial Distribution

  • 00880304367166 ()

  • 17MM
407015

  • Bone tap, reusable
Cambria Rasp, 13 x 12 x 8mm, w/Depth Stop, Flat
Seaspine Orthopedics Corporation
93-9818
In Commercial Distribution

  • 10889981093747 ()

  • 13 x 12 x 8mm
93-9818

  • Bone file/rasp, manual, reusable
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