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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
8226-0711
In Commercial Distribution

  • 00880304762190 ()

  • 7DEGX25LX11H
8226-0711

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8226-0710
In Commercial Distribution

  • 00880304762183 ()

  • 7DEGX25LX10H
8226-0710

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8226-0709
In Commercial Distribution

  • 00880304762176 ()

  • 7DEGX25LX9H
8226-0709

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8226-0708
In Commercial Distribution

  • 00880304762169 ()

  • 7DEGX25LX8H
8226-0708

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8226-0707
In Commercial Distribution

  • 00880304762152 ()

  • 7DEGX25LX7H
8226-0707

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
8417-0705
In Commercial Distribution

  • 00887868194177 ()

  • ACDF PEEK 7° 12x15x5mm
8417-0705

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8417-0510
In Commercial Distribution

  • 00887868194146 ()

  • ACDF PEEK 5° 12x15x10mm
8417-0510

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8417-0507
In Commercial Distribution

  • 00887868194115 ()

  • ACDF PEEK 5° 12x15x7mm
8417-0507

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0712
In Commercial Distribution

  • 00887868193606 ()

  • ACDF PEEK 7° 13x15x12mm
8411-0712

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0711
In Commercial Distribution

  • 00887868193590 ()

  • ACDF PEEK 7° 13x15x11mm
8411-0711

  • Polymeric spinal interbody fusion cage
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