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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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Rasp, 38mm x 26mm x 18mm, 8 Deg
Seaspine Orthopedics Corporation
95-5458
In Commercial Distribution

  • 10889981096915 ()

  • 38mm x 26mm x 18mm, 8 Deg
95-5458

  • Bone file/rasp, manual, reusable
Rasp, 38mm x 26mm x 14mm, 8 Deg
Seaspine Orthopedics Corporation
95-5454
In Commercial Distribution

  • 10889981096892 ()

  • 38mm x 26mm x 14mm, 8 Deg
95-5454

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
475616
In Commercial Distribution

  • 00880304386488 ()
475616

  • Surgical instrument handle, non-torque-limiting
Rasp, 38mm x 26mm x 10mm, 8 Deg
Seaspine Orthopedics Corporation
95-5450
In Commercial Distribution

  • 10889981096878 ()

  • 38mm x 26mm x 10mm, 8 Deg
95-5450

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
475614
In Commercial Distribution

  • 00880304386464 ()
475614

  • Manual surgical saw, rigid
Rasp, 32mm x 25mm x 16mm, 12 Deg
Seaspine Orthopedics Corporation
95-5436
In Commercial Distribution

  • 10889981096830 ()

  • 32mm x 25mm x 16mm, 12 Deg
95-5436

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
475612
In Commercial Distribution

  • 00880304386440 ()
475612

  • Surgical instrument handle, non-torque-limiting
Rasp, 32mm x 25mm x 12mm, 12 Deg
Seaspine Orthopedics Corporation
95-5432
In Commercial Distribution

  • 10889981096816 ()

  • 32mm x 25mm x 12mm, 12 Deg
95-5432

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
474892
In Commercial Distribution

  • 00880304386259 ()
474892

  • Bone-resection orthopaedic reamer, reusable
Rasp, 26mm x 24mm x 10mm, 12 Deg
Seaspine Orthopedics Corporation
95-5330
In Commercial Distribution

  • 10889981096663 ()

  • 26mm x 24mm x 10mm, 12 Deg
95-5330

  • Bone file/rasp, manual, reusable
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