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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
AR-9802C
Not in Commercial Distribution

  • B390AR9802C1 ()


  • Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed
No Description
SURETEK MEDICAL
AR-970A-90
In Commercial Distribution

  • B390AR9705A901 ()


  • Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed
No Description
SURETEK MEDICAL
AR-9705A-90
In Commercial Distribution

  • B390AR9705A90 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
AR-9703A-90
In Commercial Distribution

  • B390AR9703A901 ()


  • Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed
No Description
SURETEK MEDICAL
AC5520-01
In Commercial Distribution

  • B390AC5520011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
AC4330-01
In Commercial Distribution

  • B390AC4330011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
AC4050-01
In Commercial Distribution

  • B390AC4050011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
AC4040-01
In Commercial Distribution

  • B390AC4040011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
AC3525-01
In Commercial Distribution

  • B390AC3525011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
AC2823-01
In Commercial Distribution

  • B390AC2823011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
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