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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
8880-3212
In Commercial Distribution

  • 00888480572756 ()

  • ALIF PEEK 7° 27X36X12MM
8880-3212

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-3210
In Commercial Distribution

  • 00888480572749 ()

  • ALIF PEEK 7° 27X36X10MM
8880-3210

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-3120
In Commercial Distribution

  • 00888480572732 ()

  • ALIF PEEK 7° 24X32X20MM
8880-3120

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-3118
In Commercial Distribution

  • 00888480572725 ()

  • ALIF PEEK 7° 24X32X18MM
8880-3118

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-3116
In Commercial Distribution

  • 00888480572718 ()

  • ALIF PEEK 7° 24X32X16MM
8880-3116

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-3114
In Commercial Distribution

  • 00888480572701 ()

  • ALIF PEEK 7° 24X32X14MM
8880-3114

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-3112
In Commercial Distribution

  • 00888480572695 ()

  • ALIF PEEK 7° 24X32X12MM
8880-3112

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-3110
In Commercial Distribution

  • 00888480572688 ()

  • ALIF PEEK 7° 24X32X10MM
8880-3110

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-3108
In Commercial Distribution

  • 00888480572671 ()

  • ALIF PEEK 7° 24X32X8MM
8880-3108

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0220
In Commercial Distribution

  • 00888480572664 ()

  • ALIF PEEK 0° 27X36X20MM
8880-0220

  • Polymeric spinal interbody fusion cage
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