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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
8725-4020
In Commercial Distribution

  • 00887868208799 ()

  • 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

  • 00887868208782 ()

  • 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

  • 00887868208775 ()

  • 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

  • 00887868208768 ()

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

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

  • 00887868208744 ()

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

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8724-6050
In Commercial Distribution

  • 00887868208720 ()

  • Spacer Lat PEEK 8° CT 60L X 22W X 50H
8724-6050

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-5516
In Commercial Distribution

  • 00887868206665 ()

  • Spacer Lat PEEK 0° 55L X 22W X 16H
8721-5516

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-5512
In Commercial Distribution

  • 00887868206641 ()

  • Spacer Lat PEEK 0° 55L X 22W X 12H
8721-5512

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-5510
In Commercial Distribution

  • 00887868206634 ()

  • Spacer Lat PEEK 0° 55L X 22W X 10H
8721-5510

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-5050
In Commercial Distribution

  • 00887868206610 ()

  • Spacer Lat PEEK 0° 50L X 22W X 50H
8721-5050

  • Polymeric spinal interbody fusion cage
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