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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
8880-6118
In Commercial Distribution

  • 00888480572954 ()

  • ALIF PEEK 15° 24X32X18MM
8880-6118

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-6116
In Commercial Distribution

  • 00888480572947 ()

  • ALIF PEEK 15° 24X32X16MM
8880-6116

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-6114
In Commercial Distribution

  • 00888480572930 ()

  • ALIF PEEK 15° 24X32X14MM
8880-6114

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-6112
In Commercial Distribution

  • 00888480572923 ()

  • ALIF PEEK 15° 24X32X12MM
8880-6112

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-5220
In Commercial Distribution

  • 00888480572916 ()

  • ALIF PEEK 12° 27X36X20MM
8880-5220

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-5218
In Commercial Distribution

  • 00888480572909 ()

  • ALIF PEEK 12° 27X36X18MM
8880-5218

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-5216
In Commercial Distribution

  • 00888480572893 ()

  • ALIF PEEK 12° 27X36X16MM
8880-5216

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-5214
In Commercial Distribution

  • 00888480572886 ()

  • ALIF PEEK 12° 27X36X14MM
8880-5214

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-5212
In Commercial Distribution

  • 00888480572879 ()

  • ALIF PEEK 12° 27X36X12MM
8880-5212

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-5210
In Commercial Distribution

  • 00888480572862 ()

  • ALIF PEEK 12° 27X36X10MM
8880-5210

  • Polymeric spinal interbody fusion cage
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