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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
8725-4040
In Commercial Distribution

  • 00880304828759 ()

  • SPC LAT SPK 8DEG 40 X 22 X 40
8725-4040

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4035
In Commercial Distribution

  • 00880304828742 ()

  • SPC LAT SPK 8DEG 40 X 22 X 35
8725-4035

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4030
In Commercial Distribution

  • 00880304828735 ()

  • SPC LAT SPK 8DEG 40 X 22 X 30
8725-4030

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4025
In Commercial Distribution

  • 00880304828728 ()

  • SPC LAT SPK 8DEG 40 X 22 X 25
8725-4025

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4020
In Commercial Distribution

  • 00880304828711 ()

  • SPC LAT SPK 8DEG 40 X 22 X 20
8725-4020

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4018
In Commercial Distribution

  • 00880304828704 ()

  • SPC LAT SPK 8DEG 40 X 22 X 18
8725-4018

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4016
In Commercial Distribution

  • 00880304828698 ()

  • SPC LAT SPK 8DEG 40 X 22 X 16
8725-4016

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4014
In Commercial Distribution

  • 00880304828681 ()

  • SPC LAT SPK 8DEG 40 X 22 X 14
8725-4014

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4012
In Commercial Distribution

  • 00880304828674 ()

  • SPC LAT SPK 8DEG 40 X 22 X 12
8725-4012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8725-4010
In Commercial Distribution

  • 00880304828667 ()

  • SPC LAT SPK 8DEG 40 X 22 X 10
8725-4010

  • Polymeric spinal interbody fusion cage
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