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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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PROGAV 2.0 W/SA2.0 30 & DISTAL CATHETER
Aesculap AG
FX650T
In Commercial Distribution

  • 04041906502089 ()
FX650T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 25 & DISTAL CATHETER
Aesculap AG
FX649T
In Commercial Distribution

  • 04041906502072 ()
FX649T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 20 & DISTAL CATHETER
Aesculap AG
FX648T
In Commercial Distribution

  • 04041906502065 ()
FX648T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 15 & DISTAL CATHETER
Aesculap AG
FX647T
In Commercial Distribution

  • 04041906502058 ()
FX647T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 10 & DISTAL CATHETER
Aesculap AG
FX646T
In Commercial Distribution

  • 04041906502041 ()
FX646T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 WITH SHUNTASSISTANT 2.0 35
Aesculap AG
FX645T
In Commercial Distribution

  • 04041906502034 ()
FX645T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 WITH SHUNTASSISTANT 2.0 30
Aesculap AG
FX644T
In Commercial Distribution

  • 04041906502027 ()
FX644T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 WITH SHUNTASSISTANT 2.0 25
Aesculap AG
FX643T
In Commercial Distribution

  • 04041906502010 ()
FX643T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 WITH SHUNTASSISTANT 2.0 20
Aesculap AG
FX642T
In Commercial Distribution

  • 04041906502003 ()
FX642T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 WITH SHUNTASSISTANT 2.0 15
Aesculap AG
FX641T
In Commercial Distribution

  • 04041906501990 ()
FX641T

  • Cerebrospinal fluid shunt valve
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