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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
8825-0727
In Commercial Distribution

  • 00887868212109 ()

  • VBR PEEK 7°/0° 14x18x27mm
8825-0727

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0726
In Commercial Distribution

  • 00887868212093 ()

  • VBR PEEK 7°/0° 14x18x26mm
8825-0726

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0717
In Commercial Distribution

  • 00887868212000 ()

  • VBR PEEK 7°/0° 14x18x17mm
8825-0717

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0716
In Commercial Distribution

  • 00887868211997 ()

  • VBR PEEK 7°/0° 14x18x16mm
8825-0716

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0713
In Commercial Distribution

  • 00887868211966 ()

  • VBR PEEK 7°/0° 14x18x13mm
8825-0713

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0712
In Commercial Distribution

  • 00887868211959 ()

  • ACF PEEK 7°/0° 14x18x12mm
8825-0712

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0710
In Commercial Distribution

  • 00887868211935 ()

  • ACF PEEK 7°/0° 14x18x10mm
8825-0710

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0707
In Commercial Distribution

  • 00887868211904 ()

  • ACF PEEK 7°/0° 14x18x07mm
8825-0707

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0705
In Commercial Distribution

  • 00887868211881 ()

  • ACF PEEK 7°/0° 14x18x05mm
8825-0705

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0750
In Commercial Distribution

  • 00887868212338 ()

  • VBR PEEK 7°/0° 14x18x50mm
8825-0750

  • Polymeric spinal interbody fusion cage
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