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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M.BLUE 5 SHUNT SYSTEM
Aesculap AG
FX811T
In Commercial Distribution

  • 04041906504489 ()

  • Pressure rating horiz. (cmH2O) : 5.000 CWS
FX811T

  • Ventriculo-peritoneal/atrial shunt
M.BLUE 0 SHUNT SYSTEM
Aesculap AG
FX810T
In Commercial Distribution

  • 04041906504472 ()

  • Pressure rating horiz. (cmH2O) : 0.000 CWS
FX810T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.SPRUNG RES
Aesculap AG
FX586T
In Commercial Distribution

  • 04041906504328 ()
FX586T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.SPRUNG RES
Aesculap AG
FX585T
In Commercial Distribution

  • 04041906504311 ()
FX585T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PED.SPRUNG RES
Aesculap AG
FX584T
In Commercial Distribution

  • 04041906504304 ()
FX584T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PED.SPRUNG RES
Aesculap AG
FX583T
In Commercial Distribution

  • 04041906504298 ()
FX583T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.SPRUNG RES
Aesculap AG
FX582T
In Commercial Distribution

  • 04041906504281 ()
FX582T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.SPRUNG RES
Aesculap AG
FX581T
In Commercial Distribution

  • 04041906504274 ()
FX581T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS WITH PED.SPRUNG RESERVOIR
Aesculap AG
FX580T
In Commercial Distribution

  • 04041906504267 ()
FX580T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.SPRUNG RES
Aesculap AG
FX639T
In Commercial Distribution

  • 04041906504250 ()
FX639T

  • Ventriculo-peritoneal/atrial shunt
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