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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
142M0011
In Commercial Distribution

  • 00880304838161 ()

  • Nerve Root Retractor 11 mm
142M0011

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
142M0010
In Commercial Distribution

  • 00880304838154 ()

  • Nerve Root Retractor 10 mm
142M0010

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
142M0009
In Commercial Distribution

  • 00880304838147 ()

  • Nerve Root Retractor 9 mm
142M0009

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
142M0008
In Commercial Distribution

  • 00880304838130 ()

  • Nerve Root Retractor 8 mm
142M0008

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
142M0007
In Commercial Distribution

  • 00880304838123 ()

  • Nerve Root Retractor 7 mm
142M0007

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
142M0006
In Commercial Distribution

  • 00880304838116 ()

  • Nerve Root Retractor 6 mm
142M0006

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
142M0005
In Commercial Distribution

  • 00880304838109 ()

  • Nerve Root Retractor 5 mm
142M0005

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
131M1003
In Commercial Distribution

  • 00880304836648 ()

  • Graft Tamp Angled
131M1003

  • Surgical tamp, reusable
No Description
BIOMET SPINE LLC
131M1002
In Commercial Distribution

  • 00880304836631 ()

  • Graft Tamp Straight
131M1002

  • Surgical tamp, reusable
No Description
BIOMET SPINE LLC
LV01220
In Commercial Distribution

  • 00880304826083 ()
LV01220

  • Orthopaedic inorganic implant inserter/extractor, reusable
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