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
D5S10MZR282RT
Not in Commercial Distribution

  • 10846835004175 ()
D5S10MZR282RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D5S06AL252RT
In Commercial Distribution

  • 10846835004151 ()
D5S06AL252RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D510PR005RT
In Commercial Distribution

  • 10846835004120 ()
D510PR005RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D510P2R5155RT
In Commercial Distribution

  • 10846835004113 ()
D510P2R5155RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D510F2250RT
In Commercial Distribution

  • 10846835004106 ()
D510F2250RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D510DRP10RT
In Commercial Distribution

  • 10846835004090 ()
D510DRP10RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D508DP10RT
In Commercial Distribution

  • 10846835004069 ()
D508DP10RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D508D005RT
In Commercial Distribution

  • 10846835004038 ()
D508D005RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D505FR005RT
In Commercial Distribution

  • 10846835003994 ()
D505FR005RT

  • Cardiac mapping catheter, percutaneous, single-use
No Description
Biosense Webster Inc
D505AR005RT
In Commercial Distribution

  • 10846835003987 ()
D505AR005RT

  • Cardiac mapping catheter, percutaneous, single-use
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