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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 Type Device Class Implantable

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PROGAV 2.0 - 04041906503086

PROGAV 2.0 W/SA2.0 10 & CONTROL RESERV.
Aesculap AG
FX664T
In Commercial Distribution

  • 04041906503086 ()
FX664T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502812

PROGAV 2.0 W/SA2.0 35 & BURRHOLE RESERV.
Aesculap AG
FX382T
In Commercial Distribution

  • 04041906502812 ()
FX382T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502805

PROGAV 2.0 W/SA2.0 30 & BURRHOLE RESERV.
Aesculap AG
FX381T
In Commercial Distribution

  • 04041906502805 ()
FX381T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502799

PROGAV 2.0 W/SA2.0 25 & BURRHOLE RESERV.
Aesculap AG
FX380T
In Commercial Distribution

  • 04041906502799 ()
FX380T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502782

PROGAV 2.0 W/SA2.0 20 & BURRHOLE RESERV.
Aesculap AG
FX379T
In Commercial Distribution

  • 04041906502782 ()
FX379T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502775

PROGAV 2.0 W/SA2.0 15 & BURRHOLE RESERV.
Aesculap AG
FX378T
In Commercial Distribution

  • 04041906502775 ()
FX378T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502768

PROGAV 2.0 W/SA2.0 10 & BURRHOLE RESERV.
Aesculap AG
FX377T
In Commercial Distribution

  • 04041906502768 ()
FX377T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502492

PROGAV 2.0 W/SA2.0 35 & SPRUNG RESERVOIR
Aesculap AG
FX388T
In Commercial Distribution

  • 04041906502492 ()
FX388T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502485

PROGAV 2.0 W/SA2.0 30 & SPRUNG RESERVOIR
Aesculap AG
FX387T
In Commercial Distribution

  • 04041906502485 ()
FX387T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502478

PROGAV 2.0 W/SA2.0 25 & SPRUNG RESERVOIR
Aesculap AG
FX386T
In Commercial Distribution

  • 04041906502478 ()
FX386T

  • Cerebrospinal fluid shunt valve
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