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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
8824-3112
In Commercial Distribution

  • 00888480570387 ()

  • ACDF PEEK CONVEX 14X12X12MM
8824-3112

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-3111
In Commercial Distribution

  • 00888480570370 ()

  • ACDF PEEK CONVEX 14X12X11MM
8824-3111

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-3110
In Commercial Distribution

  • 00888480570363 ()

  • ACDF PEEK CONVEX 14X12X10MM
8824-3110

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-3109
In Commercial Distribution

  • 00888480570356 ()

  • ACDF PEEK CONVEX 14X12X9MM
8824-3109

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-3108
In Commercial Distribution

  • 00888480570349 ()

  • ACDF PEEK CONVEX 14X12X8MM
8824-3108

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-3107
In Commercial Distribution

  • 00888480570332 ()

  • ACDF PEEK CONVEX 14X12X7MM
8824-3107

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-3106
In Commercial Distribution

  • 00888480570325 ()

  • ACDF PEEK CONVEX 14X12X6MM
8824-3106

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-3105
In Commercial Distribution

  • 00888480570318 ()

  • ACDF PEEK CONVEX 14X12X5MM
8824-3105

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8814-1220
In Commercial Distribution

  • 00888480570301 ()

  • VBR PEEK 5° 12X14X20MM
8814-1220

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8814-1218
In Commercial Distribution

  • 00888480570295 ()

  • VBR PEEK 5° 12X14X18MM
8814-1218

  • Polymeric spinal interbody fusion cage
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