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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PLASMACUP FIXATION SCREW 6.5X20MM
Aesculap AG
NA770T
In Commercial Distribution

  • 04038653204472 ()

  • Length : 20.000 MM
  • Diameter (mm) : 6.500 MM
NA770T

  • Orthopaedic bone screw (non-sliding)
PLASMACUP FIXATION SCREW 6.5X16MM
Aesculap AG
NA766T
In Commercial Distribution

  • 04038653204465 ()

  • Length : 16.000 MM
  • Diameter (mm) : 6.500 MM
NA766T

  • Orthopaedic bone screw (non-sliding)
PLASMACUP FIXATION SCREW 6.5X44MM
Aesculap AG
NA794T
In Commercial Distribution

  • 04038653204533 ()

  • Length : 44.000 MM
  • Diameter (mm) : 6.500 MM
NA794T

  • Orthopaedic bone screw (non-sliding)
PLASMACUP FIXATION SCREW 6.5X36MM
Aesculap AG
NA786T
In Commercial Distribution

  • 04038653204519 ()

  • Diameter (mm) : 6.500 MM
  • Length : 36.000 MM
NA786T

  • Orthopaedic bone screw (non-sliding)
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
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 20 & PED.CONTR.RES.
Aesculap AG
FX609T
In Commercial Distribution

  • 04041906503734 ()
FX609T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PED.CONTR.RES.
Aesculap AG
FX608T
In Commercial Distribution

  • 04041906503727 ()
FX608T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PED.CONTR.RES.
Aesculap AG
FX607T
In Commercial Distribution

  • 04041906503710 ()
FX607T

  • Ventriculo-peritoneal/atrial shunt
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