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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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5mm, 4-Hole Anterior Plate
Seaspine Orthopedics Corporation
85-0705
In Commercial Distribution

  • 10889981124311 ()

  • 5mm
85-0705

  • Metal-polymer composite spinal interbody fusion cage
No Description
Biomet Orthopedics, LLC
32-483810
In Commercial Distribution

  • 00880304436510 ()

  • 20MM X 59MM
32-483810

  • Knee tibia prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
32-483890
In Commercial Distribution

  • 00880304436503 ()

  • 20MM X 87/91MM
32-483890

  • Knee tibia prosthesis trial, reusable
No Description
Biomet Orthopedics, LLC
32-483784
In Commercial Distribution

  • 00880304436497 ()

  • 14MM X 87/91MM
32-483784

  • Knee tibia prosthesis trial, reusable
8mm, 3-Hole Anterior Plate
Seaspine Orthopedics Corporation
85-0608
In Commercial Distribution

  • 10889981124267 ()

  • 8mm
85-0608

  • Metal-polymer composite spinal interbody fusion cage
No Description
Biomet Orthopedics, LLC
32-483700
In Commercial Distribution

  • 00880304436473 ()

  • 10MM X 59MM
32-483700

  • Knee tibia prosthesis trial, reusable
6mm, 3-Hole Anterior Plate
Seaspine Orthopedics Corporation
85-0606
In Commercial Distribution

  • 10889981124243 ()

  • 6mm
85-0606

  • Metal-polymer composite spinal interbody fusion cage
No Description
Biomet Orthopedics, LLC
32-483780
In Commercial Distribution

  • 00880304436459 ()

  • 10MM X 87/91MM
32-483780

  • Knee tibia prosthesis trial, reusable
12mm, 2-Hole Anterior Plate
Seaspine Orthopedics Corporation
85-0512
In Commercial Distribution

  • 10889981124229 ()

  • 12mm
85-0512

  • Metal-polymer composite spinal interbody fusion cage
11mm, 2-Hole Anterior Plate
Seaspine Orthopedics Corporation
85-0511
In Commercial Distribution

  • 10889981124212 ()

  • 11mm
85-0511

  • Metal-polymer composite spinal interbody fusion cage
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