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 SYS SA2.0 20 & PED.BURRH.RES.
Aesculap AG
FX570T
In Commercial Distribution

  • 04041906503970 ()
FX570T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.BURRH.RES.
Aesculap AG
FX569T
In Commercial Distribution

  • 04041906503963 ()
FX569T

  • 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
M.BLUE PLUS SYS W/PED.BURRHOLE RESERVOIR
Aesculap AG
FX849T
In Commercial Distribution

  • 04041906504885 ()

  • Pressure rating horiz. (cmH2O) : 0.000 - 20.000 CWS
FX849T

  • Ventriculo-peritoneal/atrial shunt
M.BLUE PLUS SYS W/PED.SPRUNG RESERVOIR
Aesculap AG
FX839T
In Commercial Distribution

  • 04041906504861 ()

  • Pressure rating horiz. (cmH2O) : 0.000 - 20.000 CWS
FX839T

  • Ventriculo-peritoneal/atrial shunt
M.BLUE 0 SHUNT SYSTEM
Aesculap AG
FX810T
In Commercial Distribution

  • 04041906504472 ()

  • Pressure rating horiz. (cmH2O) : 0.000 CWS
FX810T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.SPRUNG RES
Aesculap AG
FX586T
In Commercial Distribution

  • 04041906504328 ()
FX586T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.SPRUNG RES
Aesculap AG
FX585T
In Commercial Distribution

  • 04041906504311 ()
FX585T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.SPRUNG RES
Aesculap AG
FX584T
In Commercial Distribution

  • 04041906504304 ()
FX584T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.SPRUNG RES
Aesculap AG
FX583T
In Commercial Distribution

  • 04041906504298 ()
FX583T

  • Ventriculo-peritoneal/atrial shunt
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