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 15 & PED.BURRH.RES.
Aesculap AG
FX621T
In Commercial Distribution

  • 04041906504144 ()
FX621T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.BURRH.RES.
Aesculap AG
FX620T
In Commercial Distribution

  • 04041906504137 ()
FX620T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.BURRH.RES.
Aesculap AG
FX573T
In Commercial Distribution

  • 04041906504007 ()
FX573T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.BURRH.RES.
Aesculap AG
FX572T
In Commercial Distribution

  • 04041906503994 ()
FX572T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.BURRH.RES.
Aesculap AG
FX571T
In Commercial Distribution

  • 04041906503987 ()
FX571T

  • 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 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 30 & PED.CONTR.RES.
Aesculap AG
FX611T
In Commercial Distribution

  • 04041906503758 ()
FX611T

  • Ventriculo-peritoneal/atrial shunt
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