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 15 SHUNT SYSTEM
Aesculap AG
FX813T
In Commercial Distribution

  • 04041906504502 ()

  • Pressure rating horiz. (cmH2O) : 15.000 CWS
FX813T

  • Ventriculo-peritoneal/atrial shunt
M.BLUE 10 SHUNT SYSTEM
Aesculap AG
FX812T
In Commercial Distribution

  • 04041906504496 ()

  • Pressure rating horiz. (cmH2O) : 10.000 CWS
FX812T

  • Ventriculo-peritoneal/atrial shunt
M.BLUE 5 SHUNT SYSTEM
Aesculap AG
FX811T
In Commercial Distribution

  • 04041906504489 ()

  • Pressure rating horiz. (cmH2O) : 5.000 CWS
FX811T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS WITH PED.SPRUNG RESERVOIR
Aesculap AG
FX580T
In Commercial Distribution

  • 04041906504267 ()
FX580T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.SPRUNG RES
Aesculap AG
FX639T
In Commercial Distribution

  • 04041906504250 ()
FX639T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.SPRUNG RES
Aesculap AG
FX638T
In Commercial Distribution

  • 04041906504243 ()
FX638T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.SPRUNG RES
Aesculap AG
FX637T
In Commercial Distribution

  • 04041906504236 ()
FX637T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.SPRUNG RES
Aesculap AG
FX636T
In Commercial Distribution

  • 04041906504229 ()
FX636T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.SPRUNG RES
Aesculap AG
FX635T
In Commercial Distribution

  • 04041906504212 ()
FX635T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.SPRUNG RES
Aesculap AG
FX634T
In Commercial Distribution

  • 04041906504205 ()
FX634T

  • Ventriculo-peritoneal/atrial shunt
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