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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
101M2109
In Commercial Distribution

  • 00880304863460 ()

  • Straight Titanium Spacer Convex 21L x 09H x 10W 0°
101M2109

  • Spinal implant trial
No Description
BIOMET SPINE LLC
101M2108
In Commercial Distribution

  • 00880304863453 ()

  • Straight Titanium Spacer Convex 21L x 08H x 10W 0°
101M2108

  • Spinal implant trial
No Description
BIOMET SPINE LLC
101M2107
In Commercial Distribution

  • 00880304863446 ()

  • Straight Titanium Spacer Convex 21L x 07H x 10W 0°
101M2107

  • Spinal implant trial
No Description
BIOMET SPINE LLC
137M0003
In Commercial Distribution

  • 00880304856875 ()

  • Inner Shaft, Standard Inserter
137M0003

  • Spinal implant trial
No Description
BIOMET SPINE LLC
137M0002
In Commercial Distribution

  • 00880304856868 ()

  • Outer Shaft, Standard Inserter
137M0002

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8245-0001
In Commercial Distribution

  • 00880304819832 ()

  • ZYS TRANSFORM INSERTER
8245-0001

  • Orthopaedic inorganic implant inserter/extractor, reusable
No Description
BIOMET SPINE LLC
8228-0714
In Commercial Distribution

  • 00880304814660 ()

  • 7DEGX35LX14H
8228-0714

  • Polymeric spinal fusion cage, sterile
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
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