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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
8701-2540
In Commercial Distribution

  • 00888480561118 ()

  • SPACER LAT PEEK 25L X 16W X 40H
8701-2540

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2535
In Commercial Distribution

  • 00888480561101 ()

  • SPACER LAT PEEK 25L X 16W X 35H
8701-2535

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2530
In Commercial Distribution

  • 00888480561095 ()

  • SPACER LAT PEEK 25L X 16W X 30H
8701-2530

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2525
In Commercial Distribution

  • 00888480561088 ()

  • SPACER LAT PEEK 25L X 16W X 25H
8701-2525

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2520
In Commercial Distribution

  • 00888480561071 ()

  • SPACER LAT PEEK 25L X 16W X 20H
8701-2520

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2518
In Commercial Distribution

  • 00888480561064 ()

  • SPACER LAT PEEK 25L X 16W X 18H
8701-2518

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2516
In Commercial Distribution

  • 00888480561057 ()

  • SPACER LAT PEEK 25L X 16W X 16H
8701-2516

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2514
In Commercial Distribution

  • 00888480561040 ()

  • SPACER LAT PEEK 25L X 16W X 14H
8701-2514

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2512
In Commercial Distribution

  • 00888480561033 ()

  • SPACER LAT PEEK 25L X 16W X 12H
8701-2512

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2510
In Commercial Distribution

  • 00888480561026 ()

  • SPACER LAT PEEK 25L X 16W X 10H
8701-2510

  • Polymeric spinal interbody fusion cage
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