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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 Type Device Class Implantable

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No Description
BIOMET SPINE LLC
8228-0708
In Commercial Distribution

  • 00880304814608 ()

  • 7DEGX35LX8H
8228-0708

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8228-0707
In Commercial Distribution

  • 00880304814592 ()

  • 7DEGX35LX7H
8228-0707

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
137M0020
In Commercial Distribution

  • 00880304851498 ()

  • Inner Shaft, C-Clamp
137M0020

  • Spinal implant trial
No Description
BIOMET SPINE LLC
137M0017
In Commercial Distribution

  • 00880304851474 ()

  • Med Slap Hammer Adapter Fork
137M0017

  • Orthopaedic surgical procedure kit, non-medicated, reusable
No Description
BIOMET SPINE LLC
137M0015
In Commercial Distribution

  • 00880304851450 ()

  • 90° Reposition Hook
137M0015

  • General internal orthopaedic fixation system implantation kit
No Description
BIOMET SPINE LLC
136M3316
In Commercial Distribution

  • 00880304851290 ()

  • Curved Trial 33L x 16H x 11W mm Parallel
136M3316

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M3315
In Commercial Distribution

  • 00880304851283 ()

  • Curved Trial 33L x 15H x 11W mm Parallel
136M3315

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M3314
In Commercial Distribution

  • 00880304851276 ()

  • Curved Trial 33L x 14H x 11W mm Parallel
136M3314

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M3313
In Commercial Distribution

  • 00880304851269 ()

  • Curved Trial 33L x 13H x 11W mm Parallel
136M3313

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M3312
In Commercial Distribution

  • 00880304851252 ()

  • Curved Trial 33L x 12H x 10W mm Parallel
136M3312

  • Spinal implant trial
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