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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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PTFE CTD NEEDLE EXT INS 6'
MEDLINE INDUSTRIES, INC.
P0016M
In Commercial Distribution

  • 40888277754059 ()
  • 10888277754058 ()
P0016M

  • Endoscopic electrosurgical electrode, bipolar, single-use
PTFE COATED BLADE 6'
MEDLINE INDUSTRIES, INC.
P0014M
In Commercial Distribution

  • 40888277754042 ()
  • 10888277754041 ()
P0014M

  • Endoscopic electrosurgical electrode, bipolar, single-use
ELECTRODE PTFE BLADE 6'
MEDLINE INDUSTRIES, INC.
P0014
In Commercial Distribution

  • 40888277754035 ()
  • 10888277754034 ()
P0014

  • Endoscopic electrosurgical electrode, bipolar, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5026
In Commercial Distribution

  • 10841912101174 ()
  • 00841912101177 ()
LNGC1619FX

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5025
In Commercial Distribution

  • 10841912101167 ()
  • 00841912101160 ()
LNGC14GX

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
4742
In Commercial Distribution

  • 10841912101150 ()
  • 00841912101153 ()
4742

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
4025
In Commercial Distribution

  • 10841912101082 ()
  • 00841912101085 ()
4025

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
4023
In Commercial Distribution

  • 10841912101075 ()
  • 00841912101078 ()
4023

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
4022/TL
In Commercial Distribution

  • 00841912101061 ()
4022/TL

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
4022
In Commercial Distribution

  • 10841912101051 ()
  • 00841912101054 ()
4022

  • Needle guide, single-use
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