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
D708RHISRT
In Commercial Distribution

  • 10846835004861 ()
D708RHISRT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D708DL002RT
In Commercial Distribution

  • 10846835004823 ()
D708DL002RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D706DR002RT
In Commercial Distribution

  • 10846835004762 ()
D706DR002RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D6T20282RT
In Commercial Distribution

  • 10846835004564 ()
D6T20282RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D6S270L252RT
In Commercial Distribution

  • 10846835004557 ()
D6S270L252RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D6S08DRPRYRT
In Commercial Distribution

  • 10846835004526 ()
D6S08DRPRYRT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D6FR252RT
In Commercial Distribution

  • 10846835004502 ()
D6FR252RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D6DR252CT
In Commercial Distribution

  • 10846835004458 ()
D6DR252CT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D6DR005CT
In Commercial Distribution

  • 10846835004434 ()
D6DR005CT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D610FR252RT
In Commercial Distribution

  • 10846835004335 ()
D610FR252RT

  • Cardiac mapping catheter, percutaneous, single-use
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