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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
14-530580
In Commercial Distribution

  • 00880304911222 ()

  • ENCLAVE 20 MM, 12° WIDE 40W X 28D
14-530580

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
14-530578
In Commercial Distribution

  • 00880304911208 ()

  • ENCLAVE 18 MM, 12° WIDE 40W X 28D
14-530578

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
14-530576
In Commercial Distribution

  • 00880304911185 ()

  • ENCLAVE 16 MM, 12° WIDE 40W X 28D
14-530576

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
14-530574
In Commercial Distribution

  • 00880304911161 ()

  • ENCLAVE 14 MM, 12° WIDE 40W X 28D
14-530574

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
14-530572
In Commercial Distribution

  • 00880304911147 ()

  • ENCLAVE 12 MM, 12° WIDE 40W X 28D
14-530572

  • Vertebral body prosthesis
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