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
D8BTCJ5L
Not in Commercial Distribution

  • 10846835006551 ()
D8BTCJ5L

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D8BTCG5L
In Commercial Distribution

  • 10846835006513 ()
D8BTCG5L

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D8BTCF5L252RT
Not in Commercial Distribution

  • 10846835006483 ()
D8BTCF5L252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D8BTCE5L252RT
Not in Commercial Distribution

  • 10846835006469 ()
D8BTCE5L252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7T20282CT
In Commercial Distribution

  • 10846835005981 ()
D7T20282CT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D7R20P14RT
In Commercial Distribution

  • 10846835005950 ()
D7R20P14RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D7R20P14CT
In Commercial Distribution

  • 10846835005936 ()
D7R20P14CT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D7R20LCSRT
Not in Commercial Distribution

  • 10846835005929 ()
D7R20LCSRT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D7L2030RT
In Commercial Distribution

  • 10846835005882 ()
D7L2030RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D7L2025RT
In Commercial Distribution

  • 10846835005875 ()
D7L2025RT

  • Cardiac mapping catheter, percutaneous, single-use
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