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
D7BTCCL252RT
In Commercial Distribution

  • 10846835005196 ()
D7BTCCL252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7BTCC5L252RT
Not in Commercial Distribution

  • 10846835005189 ()
D7BTCC5L252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7BTCBL252RT
In Commercial Distribution

  • 10846835005172 ()
D7BTCBL252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7BTCB5L252RT
Not in Commercial Distribution

  • 10846835005165 ()
D7BTCB5L252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7BTBL252RT
In Commercial Distribution

  • 10846835005141 ()
D7BTBL252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7A20131RT
In Commercial Distribution

  • 10846835005042 ()
D7A20131RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D728260RT
In Commercial Distribution

  • 10846835004960 ()
D728260RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D710DRP10CT
In Commercial Distribution

  • 10846835004878 ()
D710DRP10CT

  • Cardiac mapping catheter, percutaneous, single-use
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
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