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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
8830-2313
In Commercial Distribution

  • 00888480571711 ()

  • PLIF THREADED PEEK 0° 10X23X13MM
8830-2313

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2312
In Commercial Distribution

  • 00888480571704 ()

  • PLIF THREADED PEEK 0° 10X23X12MM
8830-2312

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2311
In Commercial Distribution

  • 00888480571698 ()

  • PLIF THREADED PEEK 0° 10X23X11MM
8830-2311

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2310
In Commercial Distribution

  • 00888480571681 ()

  • PLIF THREADED PEEK 0° 10X23X10MM
8830-2310

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2309
In Commercial Distribution

  • 00888480571674 ()

  • PLIF THREADED PEEK 0° 10X23X9MM
8830-2309

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2308
In Commercial Distribution

  • 00888480571667 ()

  • PLIF THREADED PEEK 0° 10X23X8MM
8830-2308

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2307
In Commercial Distribution

  • 00888480571650 ()

  • PLIF THREADED PEEK 0° 10X23X7MM
8830-2307

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2714
In Commercial Distribution

  • 00888480571643 ()

  • PLIF CHANNELED PEEK 0° 10X27X14MM
8829-2714

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2713
In Commercial Distribution

  • 00888480571636 ()

  • PLIF CHANNELED PEEK 0° 10X27X13MM
8829-2713

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2712
In Commercial Distribution

  • 00888480571629 ()

  • PLIF CHANNELED PEEK 0° 10X27X12MM
8829-2712

  • Polymeric spinal interbody fusion cage
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