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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 Device Size Type Device Class Implantable

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CONDUIT HC150-12 HKI MO 10L
MEDTRONIC, INC.
HC150-12
In Commercial Distribution

  • 00681490908726 ()

  • Valve Size 12 MM


  • Synthetic vascular graft
Superion Dilator 1
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000369 ()
100-9146

  • Lumbar interspinous decompression instrument set, reusable
Superion Handle
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000352 ()
100-9139

  • Lumbar interspinous decompression instrument set, reusable
Superion Cannula
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000345 ()
100-9137

  • Lumbar interspinous decompression instrument set, reusable
Superion Dilator 2
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000338 ()
100-9136

  • Lumbar interspinous decompression instrument set, reusable
SuperionDilator 1, Blunt
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000321 ()
100-9135

  • Lumbar interspinous decompression instrument set, reusable
Superion Mallet
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000208 ()
100-9127

  • Lumbar interspinous decompression instrument set, reusable
Superion Retractor
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000192 ()
100-9126

  • Lumbar interspinous decompression instrument set, reusable
Superion Sterilization Tray
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000185 ()
100-9119

  • Lumbar interspinous decompression instrument set, reusable
Superion Interspinous Reamer
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000178 ()
100-9117

  • Lumbar interspinous decompression instrument set, reusable
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