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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
8833-2009
In Commercial Distribution

  • 00888480571834 ()

  • PLIF THREADED PEEK 6° 10X20X9MM
8833-2009

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8833-2008
In Commercial Distribution

  • 00888480571827 ()

  • PLIF THREADED PEEK 6° 10X20X8MM
8833-2008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8833-2007
In Commercial Distribution

  • 00888480571810 ()

  • PLIF THREADED PEEK 6° 10X20X7MM
8833-2007

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2714
In Commercial Distribution

  • 00888480571803 ()

  • PLIF THREADED PEEK 0° 10X27X14MM
8830-2714

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2713
In Commercial Distribution

  • 00888480571797 ()

  • PLIF THREADED PEEK 0° 10X27X13MM
8830-2713

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2712
In Commercial Distribution

  • 00888480571780 ()

  • PLIF THREADED PEEK 0° 10X27X12MM
8830-2712

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2711
In Commercial Distribution

  • 00888480571773 ()

  • PLIF THREADED PEEK 0° 10X27X11MM
8830-2711

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2710
In Commercial Distribution

  • 00888480571766 ()

  • PLIF THREADED PEEK 0° 10X27X10MM
8830-2710

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2709
In Commercial Distribution

  • 00888480571759 ()

  • PLIF THREADED PEEK 0° 10X27X9MM
8830-2709

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2708
In Commercial Distribution

  • 00888480571742 ()

  • PLIF THREADED PEEK 0° 10X27X8MM
8830-2708

  • Polymeric spinal interbody fusion cage
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