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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
8601-5016
In Commercial Distribution

  • 00887868196614 ()

  • Spacer MPF PEEK 0° 50L x 18W x 16Hmm
8601-5016

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8601-5014
In Commercial Distribution

  • 00887868196607 ()

  • Spacer MPF PEEK 0° 50L x 18W x 14Hmm
8601-5014

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8601-4508
In Commercial Distribution

  • 00887868196522 ()

  • Spacer MPF PEEK 0° 45L x 18W x 8Hmm
8601-4508

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8601-4014
In Commercial Distribution

  • 00887868196508 ()

  • Spacer MPF PEEK 0° 40L x 18W x 14Hmm
8601-4014

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8601-4012
In Commercial Distribution

  • 00887868196492 ()

  • Spacer MPF PEEK 0° 40L x 18W x 12Hmm
8601-4012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8518-1518
In Commercial Distribution

  • 00887868196256 ()

  • ALIF PEEK 15° 30x40x18mm
8518-1518

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8518-1516
In Commercial Distribution

  • 00887868196249 ()

  • ALIF PEEK 15° 30x40x16mm
8518-1516

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8518-1514
In Commercial Distribution

  • 00887868196232 ()

  • ALIF PEEK 15° 30x40x14mm
8518-1514

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8517-1512
In Commercial Distribution

  • 00887868196027 ()

  • ALIF PEEK Ti Marker 15° 30x40x12mm
8517-1512

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8517-1220
In Commercial Distribution

  • 00887868196010 ()

  • ALIF PEEK Ti Marker 12.5° 30x40x20mm
8517-1220

  • Polymeric spinal interbody fusion cage
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