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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
8858-2508
In Commercial Distribution

  • 00888480572305 ()

  • TLIF THREADED PEEK 0° 9X25X8MM
8858-2508

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-2507
In Commercial Distribution

  • 00888480572299 ()

  • TLIF THREADED PEEK 0° 9X25X7MM
8858-2507

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-3214
In Commercial Distribution

  • 00888480572282 ()

  • OLIF PEEK 13X32X14MM
8841-3214

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-3213
In Commercial Distribution

  • 00888480572275 ()

  • OLIF PEEK 13X32X13MM
8841-3213

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-3212
In Commercial Distribution

  • 00888480572268 ()

  • OLIF PEEK 13X32X12MM
8841-3212

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-3211
In Commercial Distribution

  • 00888480572251 ()

  • OLIF PEEK 13X32X11MM
8841-3211

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-3210
In Commercial Distribution

  • 00888480572244 ()

  • OLIF PEEK 13X32X10MM
8841-3210

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-3209
In Commercial Distribution

  • 00888480572237 ()

  • OLIF PEEK 13X32X9MM
8841-3209

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-3208
In Commercial Distribution

  • 00888480572220 ()

  • OLIF PEEK 13X32X8MM
8841-3208

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8841-3207
In Commercial Distribution

  • 00888480572213 ()

  • OLIF PEEK 13X32X7MM
8841-3207

  • Polymeric spinal interbody fusion cage
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