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 WITH BURRHOLE RESERVOIR
Aesculap AG
FX613T
In Commercial Distribution

  • 04041906502881 ()
FX613T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & BURRHOLE RES.
Aesculap AG
FX567T
In Commercial Distribution

  • 04041906502751 ()
FX567T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & BURRHOLE RES.
Aesculap AG
FX566T
In Commercial Distribution

  • 04041906502744 ()
FX566T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & BURRHOLE RES.
Aesculap AG
FX565T
In Commercial Distribution

  • 04041906502737 ()
FX565T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & BURRHOLE RES.
Aesculap AG
FX564T
In Commercial Distribution

  • 04041906502720 ()
FX564T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & BURRHOLE RES.
Aesculap AG
FX563T
In Commercial Distribution

  • 04041906502713 ()
FX563T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & BURRHOLE RES.
Aesculap AG
FX562T
In Commercial Distribution

  • 04041906502706 ()
FX562T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS WITH BURRHOLE RESERVOIR
Aesculap AG
FX690T
In Commercial Distribution

  • 04041906502690 ()
FX690T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & SPRUNG RESERV.
Aesculap AG
FX632T
In Commercial Distribution

  • 04041906502621 ()
FX632T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & SPRUNG RESERV.
Aesculap AG
FX631T
In Commercial Distribution

  • 04041906502614 ()
FX631T

  • Ventriculo-peritoneal/atrial shunt
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