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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
8725-5550
In Commercial Distribution

  • 00880304829169 ()

  • SPC LAT SPK 8DEG 55 X 22 X 50
8725-5550

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5545
In Commercial Distribution

  • 00880304829152 ()

  • SPC LAT SPK 8DEG 55 X 22 X 45
8725-5545

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5540
In Commercial Distribution

  • 00880304829145 ()

  • SPC LAT SPK 8DEG 55 X 22 X 40
8725-5540

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5535
In Commercial Distribution

  • 00880304829138 ()

  • SPC LAT SPK 8DEG 55 X 22 X 35
8725-5535

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5530
In Commercial Distribution

  • 00880304829121 ()

  • SPC LAT SPK 8DEG 55 X 22 X 30
8725-5530

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5525
In Commercial Distribution

  • 00880304829114 ()

  • SPC LAT SPK 8DEG 55 X 22 X 25
8725-5525

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5520
In Commercial Distribution

  • 00880304829107 ()

  • SPC LAT SPK 8DEG 55 X 22 X 20
8725-5520

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5518
In Commercial Distribution

  • 00880304829091 ()

  • SPC LAT SPK 8DEG 55 X 22 X 18
8725-5518

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5516
In Commercial Distribution

  • 00880304829084 ()

  • SPC LAT SPK 8DEG 55 X 22 X 16
8725-5516

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-5514
In Commercial Distribution

  • 00880304829077 ()

  • SPC LAT SPK 8DEG 55 X 22 X 14
8725-5514

  • Polymeric spinal interbody fusion cage
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