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
Biosense Webster Inc
F5CQD252RT
Not in Commercial Distribution

  • 10846835007091 ()
F5CQD252RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F5CQD005RT
In Commercial Distribution

  • 10846835007084 ()
F5CQD005RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F5CQA252RT
In Commercial Distribution

  • 10846835007077 ()
F5CQA252RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F5CQA005RT
In Commercial Distribution

  • 10846835007060 ()
F5CQA005RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F5BF010RT
In Commercial Distribution

  • 10846835007039 ()
F5BF010RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F5ADPP10RT
In Commercial Distribution

  • 10846835007008 ()
F5ADPP10RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F5ADP282CT
In Commercial Distribution

  • 10846835006971 ()
F5ADP282CT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F4SHH252RT
In Commercial Distribution

  • 10846835006933 ()
F4SHH252RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F4QH005RT
In Commercial Distribution

  • 10846835006919 ()
F4QH005RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
F4QF005RT
In Commercial Distribution

  • 10846835006902 ()
F4QF005RT

  • Cardiac mapping catheter, percutaneous, single-use
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