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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
8829-2709
In Commercial Distribution

  • 00888480571599 ()

  • PLIF CHANNELED PEEK 0° 10X27X9MM
8829-2709

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2708
In Commercial Distribution

  • 00888480571582 ()

  • PLIF CHANNELED PEEK 0° 10X27X8MM
8829-2708

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2314
In Commercial Distribution

  • 00888480571568 ()

  • PLIF CHANNELED PEEK 0° 10X23X14MM
8829-2314

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2313
In Commercial Distribution

  • 00888480571551 ()

  • PLIF CHANNELED PEEK 0° 10X23X13MM
8829-2313

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2312
In Commercial Distribution

  • 00888480571544 ()

  • PLIF CHANNELED PEEK 0° 10X23X12MM
8829-2312

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2311
In Commercial Distribution

  • 00888480571537 ()

  • PLIF CHANNELED PEEK 0° 10X23X11MM
8829-2311

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2310
In Commercial Distribution

  • 00888480571520 ()

  • PLIF CHANNELED PEEK 0° 10X23X10MM
8829-2310

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2309
In Commercial Distribution

  • 00888480571513 ()

  • PLIF CHANNELED PEEK 0° 10X23X9MM
8829-2309

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2308
In Commercial Distribution

  • 00888480571506 ()

  • PLIF CHANNELED PEEK 0° 10X23X8MM
8829-2308

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8814-1214
In Commercial Distribution

  • 00888480570264 ()

  • VBR PEEK 5° 12X14X14MM
8814-1214

  • Polymeric spinal interbody fusion cage
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