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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
8701-3010
In Commercial Distribution

  • 00888480561163 ()

  • SPACER LAT PEEK 30L X 16W X 10H
8701-3010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3008
In Commercial Distribution

  • 00888480561156 ()

  • SPACER LAT PEEK 30L X 16W X 08H
8701-3008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-3006
In Commercial Distribution

  • 00888480561149 ()

  • SPACER LAT PEEK 30L X 16W X 06H
8701-3006

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2550
In Commercial Distribution

  • 00888480561132 ()

  • SPACER LAT PEEK 25L X 16W X 50H
8701-2550

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8701-2545
In Commercial Distribution

  • 00888480561125 ()

  • SPACER LAT PEEK 25L X 16W X 45H
8701-2545

  • Polymeric spinal interbody fusion cage
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
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