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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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
PROGAV 2.0 SYS SA2.0 10 & PED.CONTR.RES.
Aesculap AG
FX607T
In Commercial Distribution

  • 04041906503710 ()
FX607T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS WITH PED.CONTROL RESERV.
Aesculap AG
FX606T
In Commercial Distribution

  • 04041906503703 ()
FX606T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.CONTR.RES.
Aesculap AG
FX561T
In Commercial Distribution

  • 04041906503697 ()
FX561T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.CONTR.RES.
Aesculap AG
FX560T
In Commercial Distribution

  • 04041906503680 ()
FX560T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.CONTR.RES.
Aesculap AG
FX559T
In Commercial Distribution

  • 04041906503673 ()
FX559T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.CONTR.RES.
Aesculap AG
FX558T
In Commercial Distribution

  • 04041906503666 ()
FX558T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.CONTR.RES.
Aesculap AG
FX557T
In Commercial Distribution

  • 04041906503659 ()
FX557T

  • Ventriculo-peritoneal/atrial shunt
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