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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
730M1008
In Commercial Distribution

  • 00880304988576 ()

  • PROBE, THORACIC, SMALL STRAIGHT
730M1008

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
730M1007
In Commercial Distribution

  • 00880304988569 ()

  • PROBE, ILIAC
730M1007

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
730M1006
In Commercial Distribution

  • 00880304988552 ()

  • PROBE, THORACIC, CURVED
730M1006

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
730M1005
In Commercial Distribution

  • 00880304988545 ()

  • PROBE, THORACIC, STRAIGHT
730M1005

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
100M6103
In Commercial Distribution

  • 00880304988415 ()

  • Tray, Ti Interbody Optional Trials
100M6103

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
100M6101
In Commercial Distribution

  • 00880304988408 ()

  • Base, Ti Interbody Optional Trials
100M6101

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
100M6100
In Commercial Distribution

  • 00880304988392 ()

  • Case, Ti Interbody Optional Trials
100M6100

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
100M5101
In Commercial Distribution

  • 00880304988378 ()

  • Base, Ti Interbody Standard Trials
100M5101

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
100M5103
In Commercial Distribution

  • 00880304988385 ()

  • Tray, Ti Interbody Standard Trials
100M5103

  • Instrument tray, reusable
No Description
BIOMET SPINE LLC
100M5100
In Commercial Distribution

  • 00880304988361 ()

  • Case, Ti Interbody Standard Trials
100M5100

  • Instrument tray, reusable
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