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 & PED.CONTR.RES.
Aesculap AG
FX607T
In Commercial Distribution

  • 04041906503710 ()
FX607T

  • 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 10 & PED.PRECHAMBER
Aesculap AG
FX543T
In Commercial Distribution

  • 04041906503574 ()
FX543T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.PRECHAMBER
Aesculap AG
FX594T
In Commercial Distribution

  • 04041906503512 ()
FX594T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PRECHAMBER
Aesculap AG
FX537T
In Commercial Distribution

  • 04041906503451 ()
FX537T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 WITH SA2.0 10 & PRECHAMBER
Aesculap AG
FX652T
In Commercial Distribution

  • 04041906503260 ()
FX652T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 SYS SA2.0 10 & PRECHAMBER
Aesculap AG
FX588T
In Commercial Distribution

  • 04041906503024 ()
FX588T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 WITH SHUNTASSISTANT 2.0 10
Aesculap AG
FX640T
In Commercial Distribution

  • 04041906501983 ()
FX640T

  • Cerebrospinal fluid shunt valve
SHUNTASSISTANT 2.0 10 W/DISTAL CATHETER
Aesculap AG
FX118T
In Commercial Distribution

  • 04041906501624 ()
FX118T

  • Cerebrospinal fluid shunt valve
GAV 2.0 SHUNT SYSTEM 10/30
Aesculap AG
FX209T
In Commercial Distribution

  • 04041906500597 ()

  • Pressure rating horiz. (cmH2O) : 10.000 CWS
  • Pressure rating vert. (cmH2O) : 30.000 CWS
FX209T

  • Ventriculo-peritoneal/atrial shunt
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