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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
8412-0509
In Commercial Distribution

  • 00888480555667 ()

  • ACDF PEEK 5° 14X17X9MM
8412-0509

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0508
In Commercial Distribution

  • 00888480555650 ()

  • ACDF PEEK 5° 14X17X8MM
8412-0508

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0507
In Commercial Distribution

  • 00888480555643 ()

  • ACDF PEEK 5° 14X17X7MM
8412-0507

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0506
In Commercial Distribution

  • 00888480555636 ()

  • ACDF PEEK 5° 14X17X6MM
8412-0506

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0505
In Commercial Distribution

  • 00888480555629 ()

  • ACDF PEEK 5° 14X17X5MM
8412-0505

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0012
In Commercial Distribution

  • 00888480555612 ()

  • ACDF PEEK 0° 14X17X12MM
8412-0012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0011
In Commercial Distribution

  • 00888480555605 ()

  • ACDF PEEK 0° 14X17X11MM
8412-0011

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0010
In Commercial Distribution

  • 00888480555599 ()

  • ACDF PEEK 0° 14X17X10MM
8412-0010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0009
In Commercial Distribution

  • 00888480555582 ()

  • ACDF PEEK 0° 14X17X9MM
8412-0009

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0008
In Commercial Distribution

  • 00888480555575 ()

  • ACDF PEEK 0° 14X17X8MM
8412-0008

  • Polymeric spinal interbody fusion cage
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