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 Type Device Class Implantable

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PROGAV 2.0 SYS WITH PED.CONTROL RESERV.
Aesculap AG
FX606T
In Commercial Distribution

  • 04041906503703 ()
FX606T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.CONTR.RES.
Aesculap AG
FX561T
In Commercial Distribution

  • 04041906503697 ()
FX561T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.CONTR.RES.
Aesculap AG
FX560T
In Commercial Distribution

  • 04041906503680 ()
FX560T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.CONTR.RES.
Aesculap AG
FX559T
In Commercial Distribution

  • 04041906503673 ()
FX559T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.CONTR.RES.
Aesculap AG
FX558T
In Commercial Distribution

  • 04041906503666 ()
FX558T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.CONTR.RES.
Aesculap AG
FX557T
In Commercial Distribution

  • 04041906503659 ()
FX557T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.CONTR.RES.
Aesculap AG
FX556T
In Commercial Distribution

  • 04041906503642 ()
FX556T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.PRECHAMBER
Aesculap AG
FX548T
In Commercial Distribution

  • 04041906503628 ()
FX548T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.PRECHAMBER
Aesculap AG
FX547T
In Commercial Distribution

  • 04041906503611 ()
FX547T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.PRECHAMBER
Aesculap AG
FX546T
In Commercial Distribution

  • 04041906503604 ()
FX546T

  • Ventriculo-peritoneal/atrial shunt
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