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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
8701-4035
In Commercial Distribution

  • 00887868200403 ()

  • Spacer Lat PEEK 40L X 16W X 35H
8701-4035

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4025
In Commercial Distribution

  • 00887868200380 ()

  • Spacer Lat PEEK 40L X 16W X 25H
8701-4025

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4018
In Commercial Distribution

  • 00887868200366 ()

  • Spacer Lat PEEK 40L X 16W X 18H
8701-4018

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4014
In Commercial Distribution

  • 00887868200342 ()

  • Spacer Lat PEEK 40L X 16W X 14H
8701-4014

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4010
In Commercial Distribution

  • 00887868200328 ()

  • Spacer Lat PEEK 40L X 16W X 10H
8701-4010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4006
In Commercial Distribution

  • 00887868200304 ()

  • Spacer Lat PEEK 40L X 16W X 06H
8701-4006

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3545
In Commercial Distribution

  • 00887868200281 ()

  • Spacer Lat PEEK 35L X 16W X 45H
8701-3545

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3535
In Commercial Distribution

  • 00887868200267 ()

  • Spacer Lat PEEK 35L X 16W X 35H
8701-3535

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3525
In Commercial Distribution

  • 00887868200243 ()

  • Spacer Lat PEEK 35L X 16W X 25H
8701-3525

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3518
In Commercial Distribution

  • 00887868200229 ()

  • Spacer Lat PEEK 35L X 16W X 18H
8701-3518

  • Polymeric spinal interbody fusion cage
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