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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
8841-2313
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
No Description
BIOMET SPINE LLC
8841-2310
In Commercial Distribution

  • 00888480572084 ()

  • OLIF PEEK 10X23X10MM
8841-2310

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2309
In Commercial Distribution

  • 00888480572077 ()

  • OLIF PEEK 10X23X9MM
8841-2309

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2308
In Commercial Distribution

  • 00888480572060 ()

  • OLIF PEEK 10X23X8MM
8841-2308

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-2307
In Commercial Distribution

  • 00888480572053 ()

  • OLIF PEEK 10X23X7MM
8841-2307

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8833-2714
In Commercial Distribution

  • 00888480572046 ()

  • PLIF THREADED PEEK 6° 10X27X14MM
8833-2714

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8833-2713
In Commercial Distribution

  • 00888480572039 ()

  • PLIF THREADED PEEK 6° 10X27X13MM
8833-2713

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8833-2712
In Commercial Distribution

  • 00888480572022 ()

  • PLIF THREADED PEEK 6° 10X27X12MM
8833-2712

  • Polymeric spinal interbody fusion cage
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