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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 - 04041906502461

PROGAV 2.0 W/SA2.0 20 & SPRUNG RESERVOIR
Aesculap AG
FX385T
In Commercial Distribution

  • 04041906502461 ()
FX385T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502454

PROGAV 2.0 W/SA2.0 15 & SPRUNG RESERVOIR
Aesculap AG
FX384T
In Commercial Distribution

  • 04041906502454 ()
FX384T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502447

PROGAV 2.0 W/SA2.0 10 & SPRUNG RESERVOIR
Aesculap AG
FX383T
In Commercial Distribution

  • 04041906502447 ()
FX383T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502379

PROGAV 2.0 W/SA2.0 35 & PED.SPRUNG RES.
Aesculap AG
FX689T
In Commercial Distribution

  • 04041906502379 ()
FX689T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502362

PROGAV 2.0 W/SA2.0 30 & PED.SPRUNG RES.
Aesculap AG
FX688T
In Commercial Distribution

  • 04041906502362 ()
FX688T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502355

PROGAV 2.0 W/SA2.0 25 & PED.SPRUNG RES.
Aesculap AG
FX687T
In Commercial Distribution

  • 04041906502355 ()
FX687T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502348

PROGAV 2.0 W/SA2.0 20 & PED.SPRUNG RES.
Aesculap AG
FX686T
In Commercial Distribution

  • 04041906502348 ()
FX686T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502331

PROGAV 2.0 W/SA2.0 15 & PED.SPRUNG RES.
Aesculap AG
FX685T
In Commercial Distribution

  • 04041906502331 ()
FX685T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502324

PROGAV 2.0 W/SA2.0 10 & PED.SPRUNG RES.
Aesculap AG
FX684T
In Commercial Distribution

  • 04041906502324 ()
FX684T

  • Cerebrospinal fluid shunt valve

PROGAV 2.0 - 04041906502317

PROGAV 2.0 WITH PED.SPRUNG RESSERVOIR
Aesculap AG
FX683T
In Commercial Distribution

  • 04041906502317 ()
FX683T

  • Cerebrospinal fluid shunt valve
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