SEARCH RESULTS FOR: (*Buy Wyoming Driver*)(38521 results)

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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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Mariner MIS - 10889981212551

Final Driver
Seaspine Orthopedics Corporation
MM2-100360
In Commercial Distribution

  • 10889981212551 ()
MM2-100360

  • Surgical screwdriver, reusable

Mariner MIS - 10889981212513

Reducer Multi-Driver
Seaspine Orthopedics Corporation
MM2-100342
In Commercial Distribution

  • 10889981212513 ()
MM2-100342

  • Surgical screwdriver, reusable

Mariner MIS - 10889981212445

MIS Navigation Driver
Seaspine Orthopedics Corporation
MM2-100190
In Commercial Distribution

  • 10889981212445 ()
MM2-100190

  • Surgical screwdriver, reusable

Mariner MIS - 10889981212438

Screw Inserter
Seaspine Orthopedics Corporation
MM2-100180
In Commercial Distribution

  • 10889981212438 ()
MM2-100180

  • Surgical screwdriver, reusable

Screw Driver Bit T20 - 00688346002065

No Description
Laboratoires Bodycad Inc
027-207-100
In Commercial Distribution

  • 00688346002065 ()
027-207-100

  • Surgical screwdriver, reusable

Screw Driver Bit T15 - 00688346001044

No Description
Laboratoires Bodycad Inc
027-201-100
In Commercial Distribution

  • 00688346001044 ()
027-201-100

  • Surgical screwdriver, reusable

ERGONOMIC HEAD DRIVER - 00880304309388

No Description
Biomet Orthopedics, LLC
31-399999
In Commercial Distribution

  • 00880304309388 ()
31-399999

  • Orthopaedic implant driver

SUNDIAL(R) - 00880304302532

No Description
Biomet Orthopedics, LLC
31-108100
In Commercial Distribution

  • 00880304302532 ()
31-108100

  • Surgical screwdriver, reusable

SCREW INSERTER - 00880304288805

No Description
Biomet Orthopedics, LLC
245015
In Commercial Distribution

  • 00880304288805 ()
245015

  • Surgical screwdriver, reusable

Integra Expandable Interbody - 10889981049577

Driver. The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
Seaspine Orthopedics Corporation
98-2201
In Commercial Distribution

  • 10889981049577 ()
98-2201

  • Surgical drill guide, reusable
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