SEARCH RESULTS FOR: 怎么做假AT(5634 results)

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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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M.BLUE 10 SYS W/PED.CONTROL RESERVOIR
Aesculap AG
FX817T
In Commercial Distribution

  • 04041906504533 ()

  • Pressure rating horiz. (cmH2O) : 10.000 CWS
FX817T

  • Ventriculo-peritoneal/atrial shunt
M.BLUE 0 SYS W/PED.CONTROL RESERVOIR
Aesculap AG
FX815T
In Commercial Distribution

  • 04041906504519 ()

  • Pressure rating horiz. (cmH2O) : 0.000 CWS
FX815T

  • Ventriculo-peritoneal/atrial shunt
M.BLUE 10 SHUNT SYSTEM
Aesculap AG
FX812T
In Commercial Distribution

  • 04041906504496 ()

  • Pressure rating horiz. (cmH2O) : 10.000 CWS
FX812T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.BURRH.RES.
Aesculap AG
FX570T
In Commercial Distribution

  • 04041906503970 ()
FX570T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.BURRH.RES.
Aesculap AG
FX568T
In Commercial Distribution

  • 04041906503956 ()
FX568T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.CONTR.RES.
Aesculap AG
FX612T
In Commercial Distribution

  • 04041906503765 ()
FX612T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.CONTR.RES.
Aesculap AG
FX611T
In Commercial Distribution

  • 04041906503758 ()
FX611T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.CONTR.RES.
Aesculap AG
FX610T
In Commercial Distribution

  • 04041906503741 ()
FX610T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.CONTR.RES.
Aesculap AG
FX609T
In Commercial Distribution

  • 04041906503734 ()
FX609T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.CONTR.RES.
Aesculap AG
FX608T
In Commercial Distribution

  • 04041906503727 ()
FX608T

  • Ventriculo-peritoneal/atrial shunt
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