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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M.BLUE PLUS VALVE
Aesculap AG
FX804T
In Commercial Distribution

  • 04041906504793 ()

  • Pressure rating horiz. (cmH2O) : 0.000 - 20.000 CWS
FX804T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 35 & PED.BURRHOLE RES
Aesculap AG
FX682T
In Commercial Distribution

  • 04041906504069 ()
FX682T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 30 & PED.BURRHOLE RES
Aesculap AG
FX681T
In Commercial Distribution

  • 04041906504052 ()
FX681T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 25 & PED.BURRHOLE RES
Aesculap AG
FX680T
In Commercial Distribution

  • 04041906504045 ()
FX680T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 20 & PED.BURRHOLE RES
Aesculap AG
FX679T
In Commercial Distribution

  • 04041906504038 ()
FX679T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 15 & PED.BURRHOLE RES
Aesculap AG
FX678T
In Commercial Distribution

  • 04041906504021 ()
FX678T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 10 & PED.BURRHOLE RES
Aesculap AG
FX677T
In Commercial Distribution

  • 04041906504014 ()
FX677T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 35 & PED.PRECHAMBER
Aesculap AG
FX663T
In Commercial Distribution

  • 04041906503826 ()
FX663T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 30 & PED.PRECHAMBER
Aesculap AG
FX662T
In Commercial Distribution

  • 04041906503819 ()
FX662T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 25 & PED.PRECHAMBER
Aesculap AG
FX661T
In Commercial Distribution

  • 04041906503802 ()
FX661T

  • Cerebrospinal fluid shunt valve
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