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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
8701-4012
In Commercial Distribution

  • 00887868200335 ()

  • Spacer Lat PEEK 40L X 16W X 12H
8701-4012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4010
In Commercial Distribution

  • 00887868200328 ()

  • Spacer Lat PEEK 40L X 16W X 10H
8701-4010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-4008
In Commercial Distribution

  • 00887868200311 ()

  • Spacer Lat PEEK 40L X 16W X 08H
8701-4008

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

  • 00887868200243 ()

  • Spacer Lat PEEK 35L X 16W X 25H
8701-3525

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

  • 00887868200229 ()

  • Spacer Lat PEEK 35L X 16W X 18H
8701-3518

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

  • 00887868200205 ()

  • Spacer Lat PEEK 35L X 16W X 14H
8701-3514

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3512
In Commercial Distribution

  • 00887868200199 ()

  • 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

  • 00887868200182 ()

  • 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

  • 00887868200175 ()

  • 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

  • 00887868200168 ()

  • Spacer Lat PEEK 35L X 16W X 06H
8701-3506

  • Polymeric spinal interbody fusion cage
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