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 25 & SPRUNG RESERV.
Aesculap AG
FX630T
In Commercial Distribution

  • 04041906502607 ()
FX630T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & SPRUNG RESERV.
Aesculap AG
FX629T
In Commercial Distribution

  • 04041906502591 ()
FX629T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & SPRUNG RESERV.
Aesculap AG
FX628T
In Commercial Distribution

  • 04041906502584 ()
FX628T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & SPRUNG RESERV.
Aesculap AG
FX627T
In Commercial Distribution

  • 04041906502577 ()
FX627T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS WITH SPRUNG RESERVOIR
Aesculap AG
FX626T
In Commercial Distribution

  • 04041906502560 ()
FX626T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & SPRUNG RESERV.
Aesculap AG
FX579T
In Commercial Distribution

  • 04041906502553 ()
FX579T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & SPRUNG RESERV.
Aesculap AG
FX578T
In Commercial Distribution

  • 04041906502546 ()
FX578T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & SPRUNG RESERV.
Aesculap AG
FX577T
In Commercial Distribution

  • 04041906502539 ()
FX577T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & SPRUNG RESERV.
Aesculap AG
FX576T
In Commercial Distribution

  • 04041906502522 ()
FX576T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & SPRUNG RESERV.
Aesculap AG
FX575T
In Commercial Distribution

  • 04041906502515 ()
FX575T

  • Ventriculo-peritoneal/atrial shunt
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