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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
8841-2812
In Commercial Distribution

  • 00888480572183 ()

  • OLIF PEEK 11X28X12MM
8841-2812

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2811
In Commercial Distribution

  • 00888480572176 ()

  • OLIF PEEK 11X28X11MM
8841-2811

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2810
In Commercial Distribution

  • 00888480572169 ()

  • OLIF PEEK 11X28X10MM
8841-2810

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2809
In Commercial Distribution

  • 00888480572152 ()

  • OLIF PEEK 11X28X9MM
8841-2809

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2808
In Commercial Distribution

  • 00888480572145 ()

  • OLIF PEEK 11X28X8MM
8841-2808

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2807
In Commercial Distribution

  • 00888480572138 ()

  • OLIF PEEK 11X28X7MM
8841-2807

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2314
In Commercial Distribution

  • 00888480572121 ()

  • OLIF PEEK 10X23X14MM
8841-2314

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2313
In Commercial Distribution

  • 00888480572114 ()

  • OLIF PEEK 10X23X13MM
8841-2313

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2312
In Commercial Distribution

  • 00888480572107 ()

  • OLIF PEEK 10X23X12MM
8841-2312

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2311
In Commercial Distribution

  • 00888480572091 ()

  • OLIF PEEK 10X23X11MM
8841-2311

  • Polymeric spinal interbody fusion cage
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