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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 Class Implantable

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CURETTE-ANGLED/6.5MM CUP WIDTH DOWN-BITING/FRONT
Synthes GmbH
03.809.773
In Commercial Distribution

  • H981038097730 ()
  • 10705034725956 ()
03809773

  • Bone curette, reusable
CURETTE-ANGLED/6.5MM CUP WIDTH STRAIGHT/RIGHT
Synthes GmbH
03.809.772
In Commercial Distribution

  • H981038097720 ()
  • 10705034725949 ()
03809772

  • Bone curette, reusable
CURETTE-ANGLED/6.5MM CUP WIDTH STRAIGHT/LEFT
Synthes GmbH
03.809.771
In Commercial Distribution

  • H981038097710 ()
  • 10705034725932 ()
03809771

  • Bone curette, reusable
RASP-ANGLED RIGHT
Synthes GmbH
03.809.770
In Commercial Distribution

  • H981038097700 ()
  • 10705034725925 ()
03809770

  • Bone file/rasp, manual, reusable
RASP-ANGLED LEFT
Synthes GmbH
03.809.769
In Commercial Distribution

  • H981038097690 ()
  • 10705034725918 ()
03809769

  • Bone file/rasp, manual, reusable
RASP SINGLE-SIDED
Synthes GmbH
03.809.680
In Commercial Distribution

  • H981038096800 ()
  • 10705034725635 ()
03809680

  • Bone file/rasp, manual, reusable
PUSH-PULL CURETTE-10 DEG
Synthes GmbH
03.809.679
In Commercial Distribution

  • H981038096790 ()
  • 10705034725628 ()
03809679

  • Bone curette, reusable
PUSH-PULL CURETTE-STRAIGHT
Synthes GmbH
03.809.678
In Commercial Distribution

  • H981038096780 ()
  • 10705034725611 ()
03809678

  • Bone curette, reusable
ALIF TRIAL SPACER RASP-QUICK RELEASE 21MM HEIGHT
Synthes GmbH
03.808.108
In Commercial Distribution

  • H981038081080 ()
  • 10705034724430 ()
03808108

  • Bone file/rasp, manual, reusable
ALIF TRIAL SPACER RASP-QUICK RELEASE 19MM HEIGHT
Synthes GmbH
03.808.107
In Commercial Distribution

  • H981038081070 ()
  • 10705034724423 ()
03808107

  • Bone file/rasp, manual, reusable
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