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 10 SYS W/PED.CONTROL RESERVOIR
Aesculap AG
FX817T
In Commercial Distribution

  • 04041906504533 ()

  • Pressure rating horiz. (cmH2O) : 10.000 CWS
FX817T

  • Ventriculo-peritoneal/atrial shunt
M.BLUE 10 VALVE W/PERITONEAL CATHETER
Aesculap AG
FX807T
In Commercial Distribution

  • 04041906504458 ()

  • Pressure rating horiz. (cmH2O) : 10.000 CWS
FX807T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 SYS SA2.0 10 & PED.BURRH.RES.
Aesculap AG
FX620T
In Commercial Distribution

  • 04041906504137 ()
FX620T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.BURRH.RES.
Aesculap AG
FX568T
In Commercial Distribution

  • 04041906503956 ()
FX568T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 W/SA2.0 10 & PED.PRECHAMBER
Aesculap AG
FX658T
In Commercial Distribution

  • 04041906503772 ()
FX658T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 SYS SA2.0 10 & PED.CONTR.RES.
Aesculap AG
FX607T
In Commercial Distribution

  • 04041906503710 ()
FX607T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.CONTR.RES.
Aesculap AG
FX556T
In Commercial Distribution

  • 04041906503642 ()
FX556T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.PRECHAMBER
Aesculap AG
FX543T
In Commercial Distribution

  • 04041906503574 ()
FX543T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.PRECHAMBER
Aesculap AG
FX594T
In Commercial Distribution

  • 04041906503512 ()
FX594T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PRECHAMBER
Aesculap AG
FX537T
In Commercial Distribution

  • 04041906503451 ()
FX537T

  • Ventriculo-peritoneal/atrial shunt
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