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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
8701-3550
In Commercial Distribution

  • 00888480561415 ()

  • SPACER LAT PEEK 35L X 16W X 50H
8701-3550

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3545
In Commercial Distribution

  • 00888480561408 ()

  • SPACER LAT PEEK 35L X 16W X 45H
8701-3545

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3540
In Commercial Distribution

  • 00888480561392 ()

  • SPACER LAT PEEK 35L X 16W X 40H
8701-3540

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3535
In Commercial Distribution

  • 00888480561385 ()

  • SPACER LAT PEEK 35L X 16W X 35H
8701-3535

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3530
In Commercial Distribution

  • 00888480561378 ()

  • SPACER LAT PEEK 35L X 16W X 30H
8701-3530

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3525
In Commercial Distribution

  • 00888480561361 ()

  • SPACER LAT PEEK 35L X 16W X 25H
8701-3525

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3520
In Commercial Distribution

  • 00888480561354 ()

  • SPACER LAT PEEK 35L X 16W X 20H
8701-3520

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3518
In Commercial Distribution

  • 00888480561347 ()

  • SPACER LAT PEEK 35L X 16W X 18H
8701-3518

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3516
In Commercial Distribution

  • 00888480561330 ()

  • SPACER LAT PEEK 35L X 16W X 16H
8701-3516

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3514
In Commercial Distribution

  • 00888480561323 ()

  • SPACER LAT PEEK 35L X 16W X 14H
8701-3514

  • Polymeric spinal interbody fusion cage
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