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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
8701-4506
In Commercial Distribution

  • 00888480561569 ()

  • SPACER LAT PEEK 45L X 16W X 06H
8701-4506

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4050
In Commercial Distribution

  • 00888480561552 ()

  • SPACER LAT PEEK 40L X 16W X 50H
8701-4050

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4045
In Commercial Distribution

  • 00888480561545 ()

  • SPACER LAT PEEK 40L X 16W X 45H
8701-4045

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4040
In Commercial Distribution

  • 00888480561538 ()

  • SPACER LAT PEEK 40L X 16W X 40H
8701-4040

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4035
In Commercial Distribution

  • 00888480561521 ()

  • SPACER LAT PEEK 40L X 16W X 35H
8701-4035

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4030
In Commercial Distribution

  • 00888480561514 ()

  • SPACER LAT PEEK 40L X 16W X 30H
8701-4030

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4025
In Commercial Distribution

  • 00888480561507 ()

  • SPACER LAT PEEK 40L X 16W X 25H
8701-4025

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4020
In Commercial Distribution

  • 00888480561491 ()

  • SPACER LAT PEEK 40L X 16W X 20H
8701-4020

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4018
In Commercial Distribution

  • 00888480561484 ()

  • SPACER LAT PEEK 40L X 16W X 18H
8701-4018

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4016
In Commercial Distribution

  • 00888480561477 ()

  • SPACER LAT PEEK 40L X 16W X 16H
8701-4016

  • Polymeric spinal interbody fusion cage
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