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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
8701-3512
In Commercial Distribution

  • 00888480561316 ()

  • SPACER LAT PEEK 35L X 16W X 12H
8701-3512

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3510
In Commercial Distribution

  • 00888480561309 ()

  • SPACER LAT PEEK 35L X 16W X 10H
8701-3510

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3508
In Commercial Distribution

  • 00888480561293 ()

  • SPACER LAT PEEK 35L X 16W X 08H
8701-3508

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3506
In Commercial Distribution

  • 00888480561286 ()

  • SPACER LAT PEEK 35L X 16W X 06H
8701-3506

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3050
In Commercial Distribution

  • 00888480561279 ()

  • SPACER LAT PEEK 30L X 16W X 50H
8701-3050

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3045
In Commercial Distribution

  • 00888480561262 ()

  • SPACER LAT PEEK 30L X 16W X 45H
8701-3045

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3040
In Commercial Distribution

  • 00888480561255 ()

  • SPACER LAT PEEK 30L X 16W X 40H
8701-3040

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3035
In Commercial Distribution

  • 00888480561248 ()

  • SPACER LAT PEEK 30L X 16W X 35H
8701-3035

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3030
In Commercial Distribution

  • 00888480561231 ()

  • SPACER LAT PEEK 30L X 16W X 30H
8701-3030

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3025
In Commercial Distribution

  • 00888480561224 ()

  • SPACER LAT PEEK 30L X 16W X 25H
8701-3025

  • Polymeric spinal interbody fusion cage
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