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 & PRECHAMBER
Aesculap AG
FX590T
In Commercial Distribution

  • 04041906503048 ()
FX590T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PRECHAMBER
Aesculap AG
FX589T
In Commercial Distribution

  • 04041906503031 ()
FX589T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PRECHAMBER
Aesculap AG
FX588T
In Commercial Distribution

  • 04041906503024 ()
FX588T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS WITH PRECHAMBER
Aesculap AG
FX587T
In Commercial Distribution

  • 04041906503017 ()
FX587T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & BURRHOLE RES.
Aesculap AG
FX619T
In Commercial Distribution

  • 04041906502942 ()
FX619T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & BURRHOLE RES.
Aesculap AG
FX618T
In Commercial Distribution

  • 04041906502935 ()
FX618T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & BURRHOLE RES.
Aesculap AG
FX617T
In Commercial Distribution

  • 04041906502928 ()
FX617T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & BURRHOLE RES.
Aesculap AG
FX616T
In Commercial Distribution

  • 04041906502911 ()
FX616T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & BURRHOLE RES.
Aesculap AG
FX615T
In Commercial Distribution

  • 04041906502904 ()
FX615T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & BURRHOLE RES.
Aesculap AG
FX614T
In Commercial Distribution

  • 04041906502898 ()
FX614T

  • Ventriculo-peritoneal/atrial shunt
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