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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
8825-0740
In Commercial Distribution

  • 00888480571384 ()

  • VBR PEEK 7°/0° 14X18X40MM
8825-0740

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0739
In Commercial Distribution

  • 00888480571377 ()

  • VBR PEEK 7°/0° 14X18X39MM
8825-0739

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0738
In Commercial Distribution

  • 00888480571360 ()

  • VBR PEEK 7°/0° 14X18X38MM
8825-0738

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0737
In Commercial Distribution

  • 00888480571353 ()

  • VBR PEEK 7°/0° 14X18X37MM
8825-0737

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0736
In Commercial Distribution

  • 00888480571346 ()

  • VBR PEEK 7°/0° 14X18X36MM
8825-0736

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0735
In Commercial Distribution

  • 00888480571339 ()

  • VBR PEEK 7°/0° 14X18X35MM
8825-0735

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0734
In Commercial Distribution

  • 00888480571322 ()

  • VBR PEEK 7°/0° 14X18X34MM
8825-0734

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0733
In Commercial Distribution

  • 00888480571315 ()

  • VBR PEEK 7°/0° 14X18X33MM
8825-0733

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0732
In Commercial Distribution

  • 00888480571308 ()

  • VBR PEEK 7°/0° 14X18X32MM
8825-0732

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0731
In Commercial Distribution

  • 00888480571292 ()

  • VBR PEEK 7°/0° 14X18X31MM
8825-0731

  • Polymeric spinal interbody fusion cage
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