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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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0.031" ID x 0.156" OD x 50 ft
BENTEC MEDICAL OPCO, LLC
BM3-1850
In Commercial Distribution

  • 00684995550049 ()


  • Surgical capillary wound drain, luminal, synthetic polymer
0.030" ID x 0.065" OD x 50 ft
BENTEC MEDICAL OPCO, LLC
BM3-1750
In Commercial Distribution

  • 00684995550032 ()


  • Surgical capillary wound drain, luminal, synthetic polymer
0.025" ID x 0.047" OD x 50 ft
BENTEC MEDICAL OPCO, LLC
BM3-1550
In Commercial Distribution

  • 00684995550025 ()


  • Surgical capillary wound drain, luminal, synthetic polymer
0.020" ID x 0.037" OD x 50 ft
BENTEC MEDICAL OPCO, LLC
BM3-1350
In Commercial Distribution

  • 00684995550018 ()


  • Surgical capillary wound drain, luminal, synthetic polymer
0.012" ID x 0.025" OD x 50 ft
BENTEC MEDICAL OPCO, LLC
BM3-1050
In Commercial Distribution

  • 00684995550001 ()


  • Surgical capillary wound drain, luminal, synthetic polymer
UNIVERSAL LIGHT GUIDES ORANGE 2MM X 8 FT
Smith & Nephew, Inc.
72204926
In Commercial Distribution

  • 00885556643754 ()
72204926

  • Fibreoptic light cable
UNIVERSAL LIGHT GUIDE ORANGE 5MM X 12 FT
Smith & Nephew, Inc.
72204925
In Commercial Distribution

  • 00885556643747 ()
72204925

  • Fibreoptic light cable
UNIVERSAL LIGHT GUIDE ORANGE 5MM X 10 FT
Smith & Nephew, Inc.
72204924
In Commercial Distribution

  • 00885556643730 ()
72204924

  • Fibreoptic light cable
UNIVERSAL LIGHT GUIDE ORANGE 5MM X 8 FT
Smith & Nephew, Inc.
72204923
In Commercial Distribution

  • 00885556643723 ()
72204923

  • Fibreoptic light cable
UNIVERSAL LIGHT GUIDE ORANGE 4MM X 10 FT
Smith & Nephew, Inc.
72204921
In Commercial Distribution

  • 00885556643709 ()
72204921

  • Fibreoptic light cable
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