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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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No Description
SURETEK MEDICAL
EICA4865-01
In Commercial Distribution

  • B390EICA4865011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA4855-01
In Commercial Distribution

  • B390EICA4855011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA4845-01
In Commercial Distribution

  • B390EICA4845011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA4835-01
In Commercial Distribution

  • B390EICA4835011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
Reprocessed Excise PDW
SURETEK MEDICAL
EIC9820-01
In Commercial Distribution

  • B390EIC9820011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EIC8898-01
In Commercial Distribution

  • B390EIC8898011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EIC8872-01
In Commercial Distribution

  • B390EIC8872011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EIC8870-01
In Commercial Distribution

  • B390EIC8870011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EIC6895-01
In Commercial Distribution

  • B390EIC6895011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EIC5874-01
In Commercial Distribution

  • B390EIC5874011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
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