SEARCH RESULTS FOR: 仿制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.SPRUNG RES
Aesculap AG
FX637T
In Commercial Distribution

  • 04041906504236 ()
FX637T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.SPRUNG RES
Aesculap AG
FX636T
In Commercial Distribution

  • 04041906504229 ()
FX636T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.SPRUNG RES
Aesculap AG
FX634T
In Commercial Distribution

  • 04041906504205 ()
FX634T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.BURRH.RES.
Aesculap AG
FX621T
In Commercial Distribution

  • 04041906504144 ()
FX621T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.BURRH.RES.
Aesculap AG
FX569T
In Commercial Distribution

  • 04041906503963 ()
FX569T

  • 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 25 & PED.CONTR.RES.
Aesculap AG
FX610T
In Commercial Distribution

  • 04041906503741 ()
FX610T

  • 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 25 & PED.PRECHAMBER
Aesculap AG
FX546T
In Commercial Distribution

  • 04041906503604 ()
FX546T

  • Ventriculo-peritoneal/atrial shunt
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