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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
8825-0707
In Commercial Distribution

  • 00887868211904 ()

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

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0706
In Commercial Distribution

  • 00887868211898 ()

  • ACF PEEK 7°/0° 14x18x06mm
8825-0706

  • 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

  • 00888480571483 ()

  • VBR PEEK 7°/0° 14X18X50MM
8825-0750

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0749
In Commercial Distribution

  • 00888480571476 ()

  • VBR PEEK 7°/0° 14X18X49MM
8825-0749

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0748
In Commercial Distribution

  • 00888480571469 ()

  • VBR PEEK 7°/0° 14X18X48MM
8825-0748

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0747
In Commercial Distribution

  • 00888480571452 ()

  • VBR PEEK 7°/0° 14X18X47MM
8825-0747

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0746
In Commercial Distribution

  • 00888480571445 ()

  • VBR PEEK 7°/0° 14X18X46MM
8825-0746

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0745
In Commercial Distribution

  • 00888480571438 ()

  • VBR PEEK 7°/0° 14X18X45MM
8825-0745

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0744
In Commercial Distribution

  • 00888480571421 ()

  • VBR PEEK 7°/0° 14X18X44MM
8825-0744

  • Polymeric spinal interbody fusion cage
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