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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
8825-0730
In Commercial Distribution

  • 00888480571285 ()

  • VBR PEEK 7°/0° 14X18X30MM
8825-0730

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0729
In Commercial Distribution

  • 00888480571278 ()

  • VBR PEEK 7°/0° 14X18X29MM
8825-0729

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0728
In Commercial Distribution

  • 00888480571261 ()

  • VBR PEEK 7°/0° 14X18X28MM
8825-0728

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0727
In Commercial Distribution

  • 00888480571254 ()

  • VBR PEEK 7°/0° 14X18X27MM
8825-0727

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

  • 00888480571247 ()

  • VBR PEEK 7°/0° 14X18X26MM
8825-0726

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0725
In Commercial Distribution

  • 00888480571230 ()

  • VBR PEEK 7°/0° 14X18X25MM
8825-0725

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0724
In Commercial Distribution

  • 00888480571223 ()

  • VBR PEEK 7°/0° 14X18X24MM
8825-0724

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0723
In Commercial Distribution

  • 00888480571216 ()

  • VBR PEEK 7°/0° 14X18X23MM
8825-0723

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0722
In Commercial Distribution

  • 00888480571209 ()

  • VBR PEEK 7°/0° 14X18X22MM
8825-0722

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0721
In Commercial Distribution

  • 00888480571193 ()

  • VBR PEEK 7°/0° 14X18X21MM
8825-0721

  • Polymeric spinal interbody fusion cage
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