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.PRECHAMBER
Aesculap AG
FX545T
In Commercial Distribution

  • 04041906503598 ()
FX545T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.PRECHAMBER
Aesculap AG
FX544T
In Commercial Distribution

  • 04041906503581 ()
FX544T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.PRECHAMBER
Aesculap AG
FX543T
In Commercial Distribution

  • 04041906503574 ()
FX543T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.PRECHAMBER
Aesculap AG
FX599T
In Commercial Distribution

  • 04041906503567 ()
FX599T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.PRECHAMBER
Aesculap AG
FX598T
In Commercial Distribution

  • 04041906503550 ()
FX598T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.PRECHAMBER
Aesculap AG
FX597T
In Commercial Distribution

  • 04041906503543 ()
FX597T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.PRECHAMBER
Aesculap AG
FX596T
In Commercial Distribution

  • 04041906503536 ()
FX596T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.PRECHAMBER
Aesculap AG
FX595T
In Commercial Distribution

  • 04041906503529 ()
FX595T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.PRECHAMBER
Aesculap AG
FX594T
In Commercial Distribution

  • 04041906503512 ()
FX594T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PRECHAMBER
Aesculap AG
FX542T
In Commercial Distribution

  • 04041906503505 ()
FX542T

  • Ventriculo-peritoneal/atrial shunt
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