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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 Device Size Type Device Class Implantable

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No Description
BIOMET SPINE LLC
8228-0713
In Commercial Distribution

  • 00880304814653 ()

  • 7DEGX35LX13H
8228-0713

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8228-0712
In Commercial Distribution

  • 00880304814646 ()

  • 7DEGX35LX12H
8228-0712

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8228-0711
In Commercial Distribution

  • 00880304814639 ()

  • 7DEGX35LX11H
8228-0711

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8228-0710
In Commercial Distribution

  • 00880304814622 ()

  • 7DEGX35LX10H
8228-0710

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8228-0709
In Commercial Distribution

  • 00880304814615 ()

  • 7DEGX35LX9H
8228-0709

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8228-0708
In Commercial Distribution

  • 00880304814608 ()

  • 7DEGX35LX8H
8228-0708

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8228-0707
In Commercial Distribution

  • 00880304814592 ()

  • 7DEGX35LX7H
8228-0707

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8227-0714
In Commercial Distribution

  • 00880304762305 ()

  • 7DEGX30LX14H
8227-0714

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8227-0713
In Commercial Distribution

  • 00880304762299 ()

  • 7DEGX30LX13H
8227-0713

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8227-0712
In Commercial Distribution

  • 00880304762282 ()

  • 7DEGX30LX12H
8227-0712

  • Polymeric spinal fusion cage, sterile
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