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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
EICA8875-01
In Commercial Distribution

  • B390EICA8875011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA8872-01
In Commercial Distribution

  • B390EICA8872011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA8870-01
In Commercial Distribution

  • B390EICA8870011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA7070-01
Not in Commercial Distribution

  • B390EICA7070011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA6895-01-X
In Commercial Distribution

  • B390EICA689501X1 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA6895-01
In Commercial Distribution

  • B390EICA6895011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA5874-01
In Commercial Distribution

  • B390EICA5874011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
EICA5872-01
In Commercial Distribution

  • B390EICA5872011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
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
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