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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
8707-5520
In Commercial Distribution

  • 00887868202940 ()

  • Spacer Lat PEEK 0° CT 55L X 26W X 20H
8707-5520

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8707-5516
In Commercial Distribution

  • 00887868202926 ()

  • Spacer Lat PEEK 0° CT 55L X 26W X 16H
8707-5516

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8707-5510
In Commercial Distribution

  • 00887868202896 ()

  • Spacer Lat PEEK 0° CT 55L X 26W X 10H
8707-5510

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8707-5045
In Commercial Distribution

  • 00887868202872 ()

  • Spacer Lat PEEK 0° CT 50L X 26W X 45H
8707-5045

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8707-5040
In Commercial Distribution

  • 00887868202865 ()

  • Spacer Lat PEEK 0° CT 50L X 26W X 40H
8707-5040

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8707-5030
In Commercial Distribution

  • 00887868202841 ()

  • Spacer Lat PEEK 0° CT 50L X 26W X 30H
8707-5030

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-6220
In Commercial Distribution

  • 00888480573012 ()

  • ALIF PEEK 15° 27X36X20MM
8880-6220

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-6218
In Commercial Distribution

  • 00888480573005 ()

  • ALIF PEEK 15° 27X36X18MM
8880-6218

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-6214
In Commercial Distribution

  • 00888480572985 ()

  • ALIF PEEK 15° 27X36X14MM
8880-6214

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-6118
In Commercial Distribution

  • 00888480572954 ()

  • ALIF PEEK 15° 24X32X18MM
8880-6118

  • Polymeric spinal interbody fusion cage
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