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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
ASC4251-01
In Commercial Distribution

  • B390ASC4251011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
ASC4250-01
In Commercial Distribution

  • B390ASC4250011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
ASC3730-01
In Commercial Distribution

  • B390ASC3730011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
ASC2530-01
In Commercial Distribution

  • B390ASC2530011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
ASC1336-01
In Commercial Distribution

  • B390ASC1336011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
AS4730-01
In Commercial Distribution

  • B390AS4730011 ()


  • Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
No Description
SURETEK MEDICAL
AR-9803A-90
In Commercial Distribution

  • B390AR9803A901 ()


  • 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-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
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