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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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LUMINARY ALIF RASP-LONG ANTERIOR 15MM
Synthes GmbH
SD398.104
In Commercial Distribution

  • H981SD3981040 ()
  • 10705034709741 ()
SD398104

  • Bone file/rasp, manual, reusable
LUMINARY ALIF RASP-LONG ANTERIOR 13MM
Synthes GmbH
SD398.103
In Commercial Distribution

  • H981SD3981030 ()
  • 10705034709734 ()
SD398103

  • Bone file/rasp, manual, reusable
LUMINARY ALIF RASP-LONG ANTERIOR 11MM
Synthes GmbH
SD398.102
In Commercial Distribution

  • H981SD3981020 ()
  • 10705034709727 ()
SD398102

  • Bone file/rasp, manual, reusable
LUMINARY ALIF RASP-LONG ANTERIOR 9MM
Synthes GmbH
SD398.101
In Commercial Distribution

  • H981SD3981010 ()
  • 10705034709710 ()
SD398101

  • Bone file/rasp, manual, reusable
LUMINARY ALIF RASP-ANTERIOR 40 DEG/17MM HEIGHT
Synthes GmbH
SD398.095
In Commercial Distribution

  • H981SD3980950 ()
  • 10705034709703 ()
SD398095

  • Bone file/rasp, manual, reusable
LUMINARY ALIF RASP-ANTERIOR 40 DEG/15MM HEIGHT
Synthes GmbH
SD398.094
In Commercial Distribution

  • H981SD3980940 ()
  • 10705034709697 ()
SD398094

  • Bone file/rasp, manual, reusable
LUMINARY ALIF RASP-ANTERIOR 40 DEG/13MM HEIGHT
Synthes GmbH
SD398.093
In Commercial Distribution

  • H981SD3980930 ()
  • 10705034709680 ()
SD398093

  • Bone file/rasp, manual, reusable
LUMINARY ALIF RASP-ANTERIOR 40 DEG/11MM HEIGHT
Synthes GmbH
SD398.092
In Commercial Distribution

  • H981SD3980920 ()
  • 10705034709673 ()
SD398092

  • Bone file/rasp, manual, reusable
TI CERVICAL SPINE LOCKING PLATE 92MM (84MM)
Synthes GmbH
450.484
In Commercial Distribution

  • H9814504840 ()
  • 10705034781730 ()
450484

  • Spinal fixation plate, non-bioabsorbable
TI CERVICAL SPINE LOCKING PLATE 88MM (80MM)
Synthes GmbH
450.480
In Commercial Distribution

  • H9814504800 ()
  • 10705034781723 ()
450480

  • Spinal fixation plate, non-bioabsorbable
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