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 SA2.0 10 & CONTROL RES.
Aesculap AG
FX549T
In Commercial Distribution

  • 04041906503147 ()
FX549T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 W/SA2.0 10 & CONTROL RESERV.
Aesculap AG
FX664T
In Commercial Distribution

  • 04041906503086 ()
FX664T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 SYS SA2.0 10 & BURRHOLE RES.
Aesculap AG
FX614T
In Commercial Distribution

  • 04041906502898 ()
FX614T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 W/SA2.0 10 & BURRHOLE RESERV.
Aesculap AG
FX377T
In Commercial Distribution

  • 04041906502768 ()
FX377T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 SYS SA2.0 10 & BURRHOLE RES.
Aesculap AG
FX562T
In Commercial Distribution

  • 04041906502706 ()
FX562T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & SPRUNG RESERV.
Aesculap AG
FX627T
In Commercial Distribution

  • 04041906502577 ()
FX627T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & SPRUNG RESERV.
Aesculap AG
FX574T
In Commercial Distribution

  • 04041906502508 ()
FX574T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 W/SA2.0 10 & SPRUNG RESERVOIR
Aesculap AG
FX383T
In Commercial Distribution

  • 04041906502447 ()
FX383T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 10 & PED.SPRUNG RES.
Aesculap AG
FX684T
In Commercial Distribution

  • 04041906502324 ()
FX684T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 10 & PED.CONTROL RES.
Aesculap AG
FX671T
In Commercial Distribution

  • 04041906502256 ()
FX671T

  • Cerebrospinal fluid shunt valve
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