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 W/SA2.0 35 & PED.SPRUNG RES.
Aesculap AG
FX689T
In Commercial Distribution

  • 04041906502379 ()
FX689T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 30 & PED.SPRUNG RES.
Aesculap AG
FX688T
In Commercial Distribution

  • 04041906502362 ()
FX688T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 25 & PED.SPRUNG RES.
Aesculap AG
FX687T
In Commercial Distribution

  • 04041906502355 ()
FX687T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 20 & PED.SPRUNG RES.
Aesculap AG
FX686T
In Commercial Distribution

  • 04041906502348 ()
FX686T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 15 & PED.SPRUNG RES.
Aesculap AG
FX685T
In Commercial Distribution

  • 04041906502331 ()
FX685T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 10 & PED.SPRUNG RES.
Aesculap AG
FX684T
In Commercial Distribution

  • 04041906502324 ()
FX684T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 WITH PED.SPRUNG RESSERVOIR
Aesculap AG
FX683T
In Commercial Distribution

  • 04041906502317 ()
FX683T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 35 & PED.CONTROL RES.
Aesculap AG
FX676T
In Commercial Distribution

  • 04041906502300 ()
FX676T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 30 & PED.CONTROL RES.
Aesculap AG
FX675T
In Commercial Distribution

  • 04041906502294 ()
FX675T

  • Cerebrospinal fluid shunt valve
PROGAV 2.0 W/SA2.0 25 & PED.CONTROL RES.
Aesculap AG
FX674T
In Commercial Distribution

  • 04041906502287 ()
FX674T

  • Cerebrospinal fluid shunt valve
< 1 ... 398 399 400 401 402 ... 564 >