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 W/SA2.0 20 & PED.CONTROL RES.
Aesculap AG
FX673T
In Commercial Distribution

  • 04041906502270 ()
FX673T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 15 & PED.CONTROL RES.
Aesculap AG
FX672T
In Commercial Distribution

  • 04041906502263 ()
FX672T

  • 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
PROGAV 2.0 WITH PED.CONTROL RESERVOIR
Aesculap AG
FX670T
In Commercial Distribution

  • 04041906502249 ()
FX670T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 35 & DISTAL CATHETER
Aesculap AG
FX651T
In Commercial Distribution

  • 04041906502096 ()
FX651T

  • Cerebrospinal fluid shunt valve
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
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