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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 w/ Stop, 8 mm
Seaspine Orthopedics Corporation
93-9328
In Commercial Distribution

  • 10889981093204 ()

  • 8mm
93-9328

  • Bone file/rasp, manual, reusable
Rasp w/ Stop, 7 mm
Seaspine Orthopedics Corporation
93-9327
In Commercial Distribution

  • 10889981093198 ()

  • 7mm
93-9327

  • Bone file/rasp, manual, reusable
Rasp w/ Stop, 6 mm
Seaspine Orthopedics Corporation
93-9326
In Commercial Distribution

  • 10889981093181 ()

  • 6mm
93-9326

  • Bone file/rasp, manual, reusable
Rasp w/ Stop, 5 mm
Seaspine Orthopedics Corporation
93-9325
In Commercial Distribution

  • 10889981093174 ()

  • 5mm
93-9325

  • Bone file/rasp, manual, reusable
Rasp, 8.5 in, 11 mm
Seaspine Orthopedics Corporation
93-9321
In Commercial Distribution

  • 10889981093150 ()

  • 8.5 in, 11 mm
93-9321

  • Bone file/rasp, manual, reusable
Rasp, 8.5 in, 9 mm
Seaspine Orthopedics Corporation
93-9319
In Commercial Distribution

  • 10889981093136 ()

  • 8.5 in, 9 mm
93-9319

  • Bone file/rasp, manual, reusable
Rasp, 8.5 in, 7 mm
Seaspine Orthopedics Corporation
93-9317
In Commercial Distribution

  • 10889981093112 ()

  • 8.5 in, 7 mm
93-9317

  • Bone file/rasp, manual, reusable
Rasp, 8.5 in, 5 mm
Seaspine Orthopedics Corporation
93-9315
In Commercial Distribution

  • 10889981093099 ()

  • 8.5 in, 5 mm
93-9315

  • Bone file/rasp, manual, reusable
Cambria Rasp, 12 mm
Seaspine Orthopedics Corporation
93-9312
In Commercial Distribution

  • 10889981093082 ()

  • 12mm
93-9312

  • Bone file/rasp, manual, reusable
Cambria Rasp, 10 mm
Seaspine Orthopedics Corporation
93-9310
In Commercial Distribution

  • 10889981093068 ()

  • 10mm
93-9310

  • Bone file/rasp, manual, reusable
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