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
D7BTEL252RT
In Commercial Distribution

  • 10846835005400 ()
D7BTEL252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7BTD5L252RT
In Commercial Distribution

  • 10846835005356 ()
D7BTD5L252RT

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7BTCJL
In Commercial Distribution

  • 10846835005318 ()
D7BTCJL

  • Cardiac radio-frequency ablation system catheter
No Description
Biosense Webster Inc
D7BTCFL252RT
In Commercial Distribution

  • 10846835005257 ()
D7BTCFL252RT

  • Cardiac radio-frequency ablation system catheter
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
BD710FJ282RTS
In Commercial Distribution

  • 10846835002430 ()
BD710FJ282RTS

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
BD710DF282CT
In Commercial Distribution

  • 10846835002409 ()
BD710DF282CT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
123703S
Not in Commercial Distribution

  • 10846835002348 ()
123703S

  • Cardiac mapping catheter, percutaneous, single-use
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