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

Show Filters

PROGAV 2.0 SYS SA2.0 10 & CONTROL RES.
Aesculap AG
FX600T
In Commercial Distribution

  • 04041906503208 ()

  • Pressure rating horiz. (cmH2O) : 0.000 - 20.000 CWS
  • Pressure rating vert. (cmH2O) : 10.000 CWS
FX600T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & CONTROL RES.
Aesculap AG
FX554T
In Commercial Distribution

  • 04041906503192 ()
FX554T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & CONTROL RES.
Aesculap AG
FX553T
In Commercial Distribution

  • 04041906503185 ()
FX553T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & CONTROL RES.
Aesculap AG
FX552T
In Commercial Distribution

  • 04041906503178 ()
FX552T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & CONTROL RES.
Aesculap AG
FX551T
In Commercial Distribution

  • 04041906503161 ()
FX551T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & CONTROL RES.
Aesculap AG
FX550T
In Commercial Distribution

  • 04041906503154 ()
FX550T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & CONTROL RES.
Aesculap AG
FX549T
In Commercial Distribution

  • 04041906503147 ()
FX549T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PRECHAMBER
Aesculap AG
FX593T
In Commercial Distribution

  • 04041906503079 ()
FX593T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PRECHAMBER
Aesculap AG
FX592T
In Commercial Distribution

  • 04041906503062 ()
FX592T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PRECHAMBER
Aesculap AG
FX591T
In Commercial Distribution

  • 04041906503055 ()
FX591T

  • Ventriculo-peritoneal/atrial shunt
< 1 ... 520 521 522 523 524 ... 564 >