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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
8880-0112
In Commercial Distribution

  • 00888480572558 ()

  • ALIF PEEK 0° 24X32X12MM
8880-0112

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0110
In Commercial Distribution

  • 00888480572541 ()

  • ALIF PEEK 0° 24X32X10MM
8880-0110

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0108
In Commercial Distribution

  • 00888480572534 ()

  • ALIF PEEK 0° 24X32X8MM
8880-0108

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-3014
In Commercial Distribution

  • 00888480572527 ()

  • TLIF CHANNELED PEEK 0° 9X30X14MM
8859-3014

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-3012
In Commercial Distribution

  • 00888480572510 ()

  • TLIF CHANNELED PEEK 0° 9X30X12MM
8859-3012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-3010
In Commercial Distribution

  • 00888480572503 ()

  • TLIF CHANNELED PEEK 0° 9X30X10MM
8859-3010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-3008
In Commercial Distribution

  • 00888480572497 ()

  • TLIF CHANNELED PEEK 0° 9X30X8MM
8859-3008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-2514
In Commercial Distribution

  • 00888480572480 ()

  • TLIF CHANNELED PEEK 0° 9X25X14MM
8859-2514

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-2512
In Commercial Distribution

  • 00888480572473 ()

  • TLIF CHANNELED PEEK 0° 9X25X12MM
8859-2512

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-2510
In Commercial Distribution

  • 00888480572466 ()

  • TLIF CHANNELED PEEK 0° 9X25X10MM
8859-2510

  • Polymeric spinal interbody fusion cage
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