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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 Implant, 15mm x 13mm x 10mm, Lordotic
Seaspine Orthopedics Corporation
39-1610
Not in Commercial Distribution

  • 10889981137274 ()

  • 15mm x 13mm x 10mm
39-1610

  • Vertebral body prosthesis, non-sterile
Cambria NM Implant, 15mm x 13mm x 8mm, Lordotic
Seaspine Orthopedics Corporation
39-1608
Not in Commercial Distribution

  • 10889981137250 ()

  • 15mm x 13mm x 8mm
39-1608

  • Vertebral body prosthesis, non-sterile
Cambria NM Implant, 15mm x 13mm x 6mm, Lordotic
Seaspine Orthopedics Corporation
39-1606
Not in Commercial Distribution

  • 10889981137236 ()

  • 15mm x 13mm x 6mm
39-1606

  • Vertebral body prosthesis, non-sterile
Cambria NM Implant, 15mm x 13mm x 5mm, Lordotic
Seaspine Orthopedics Corporation
39-1605
Not in Commercial Distribution

  • 10889981137229 ()

  • 15mm x 13mm x 5mm
39-1605

  • Vertebral body prosthesis, non-sterile
No Description
Biomet Orthopedics, LLC
32-488513
In Commercial Distribution

  • 00880304444300 ()
32-488513

  • Bone punch, reusable
No Description
Biomet Orthopedics, LLC
32-484638
In Commercial Distribution

  • 00880304465497 ()
32-484638

  • Bone punch, reusable
No Description
Biomet Orthopedics, LLC
32-484632
In Commercial Distribution

  • 00880304465480 ()
32-484632

  • Bone punch, reusable
No Description
Biomet Orthopedics, LLC
32-484633
In Commercial Distribution

  • 00880304465473 ()
32-484633

  • Bone punch, reusable
No Description
Biomet Orthopedics, LLC
32-484637
In Commercial Distribution

  • 00880304464902 ()
32-484637

  • Bone punch, reusable
Lateral Box Cutter, 6x23mm, Angled
Seaspine Orthopedics Corporation
95-6619
In Commercial Distribution

  • 10889981162641 ()

  • 6x23mm
95-6619

  • Bone file
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