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 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
PROGAV 2.0 SYS SA2.0 30 & PED.SPRUNG RES
Aesculap AG
FX638T
In Commercial Distribution

  • 04041906504243 ()
FX638T

  • Ventriculo-peritoneal/atrial shunt
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 15 & PED.SPRUNG RES
Aesculap AG
FX635T
In Commercial Distribution

  • 04041906504212 ()
FX635T

  • 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 WITH PED.SPRUNG RESERVOIR
Aesculap AG
FX633T
In Commercial Distribution

  • 04041906504199 ()
FX633T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PED.BURRH.RES.
Aesculap AG
FX625T
In Commercial Distribution

  • 04041906504182 ()
FX625T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PED.BURRH.RES.
Aesculap AG
FX624T
In Commercial Distribution

  • 04041906504175 ()
FX624T

  • Ventriculo-peritoneal/atrial shunt
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