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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
8411-0011
In Commercial Distribution

  • 00888480555360 ()

  • ACDF PEEK 0° 13X15X11MM
8411-0011

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0010
In Commercial Distribution

  • 00888480555353 ()

  • ACDF PEEK 0° 13X15X10MM
8411-0010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0009
In Commercial Distribution

  • 00888480555346 ()

  • ACDF PEEK 0° 13X15X9MM
8411-0009

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0008
In Commercial Distribution

  • 00888480555339 ()

  • ACDF PEEK 0° 13X15X8MM
8411-0008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0007
In Commercial Distribution

  • 00888480555322 ()

  • ACDF PEEK 0° 13X15X7MM
8411-0007

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0006
In Commercial Distribution

  • 00888480555315 ()

  • ACDF PEEK 0° 13X15X6MM
8411-0006

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0005
In Commercial Distribution

  • 00888480555308 ()

  • ACDF PEEK 0° 13X15X5MM
8411-0005

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8738-1114
In Commercial Distribution

  • 00888480684763 ()

  • TIMB BULLET ANG TRL 18WX14HX0DG
8738-1114

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8738-1110
In Commercial Distribution

  • 00888480684749 ()

  • TIMB BULLET ANG TRL 18WX10HX0DG
8738-1110

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8738-1220
In Commercial Distribution

  • 00888480684725 ()

  • TIMB BULLET TRL 18WX20HX8DEG
8738-1220

  • Spinal implant trial
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