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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
136M2812
In Commercial Distribution

  • 00880304851146 ()

  • Curved Trial 28L x 12H x 10W mm Parallel
136M2812

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M2811
In Commercial Distribution

  • 00880304851139 ()

  • Curved Trial 28L x 11H x 10W mm Parallel
136M2811

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M2810
In Commercial Distribution

  • 00880304851122 ()

  • Curved Trial 28L x 10H x 10W mm Parallel
136M2810

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M2809
In Commercial Distribution

  • 00880304851115 ()

  • Curved Trial 28L x 09H x 10W mm Parallel
136M2809

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M2808
In Commercial Distribution

  • 00880304851108 ()

  • Curved Trial 28L x 08H x 10W mm Parallel
136M2808

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M2807
In Commercial Distribution

  • 00880304851092 ()

  • Curved Trial 28L x 07H x 10W mm Parallel
136M2807

  • Spinal implant trial
No Description
BIOMET SPINE LLC
136M2806
In Commercial Distribution

  • 00880304851085 ()

  • Curved Trial 28L x 06H x 10W mm   Parallel
136M2806

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3315
In Commercial Distribution

  • 00880304864580 ()

  • Curved Titanium Spacer Lordotic 33L x 15H x 11W 10°
104M3315

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3314
In Commercial Distribution

  • 00880304864573 ()

  • Curved Titanium Spacer Lordotic 33L x 14H x 11W 10°
104M3314

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3313
In Commercial Distribution

  • 00880304864566 ()

  • Curved Titanium Spacer Lordotic 33L x 13H x 11W 10°
104M3313

  • Spinal implant trial
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