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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w / Pressure Limiting Valve
Ambu A/S
524611031
In Commercial Distribution

  • 05707480149742 ()
  • 05707480149735 ()
524611031

  • Pulmonary resuscitator, manual, single-use
w/PEEP Valve 20
Ambu A/S
524611011
In Commercial Distribution

  • 05707480149728 ()
  • 05707480149711 ()
524611011

  • Pulmonary resuscitator, manual, single-use
Pop-off open 40", w/PEEP Valve 20
Ambu A/S
524611001
In Commercial Distribution

  • 05707480149704 ()
  • 05707480149698 ()

  • Adult
524611001

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
523632016
In Commercial Distribution

  • 05707480149681 ()
  • 05707480149674 ()
523632016

  • Pulmonary resuscitator, manual, single-use
w/ Exhalation Filter
Ambu A/S
523616017
In Commercial Distribution

  • 05707480149667 ()
  • 05707480149650 ()
523616017

  • Pulmonary resuscitator, manual, single-use
w/CO2 Detector , Mercury Filter, PEEP, Manometer
Ambu A/S
523611751
In Commercial Distribution

  • 05707480149643 ()
  • 05707480149636 ()
523611751

  • Pulmonary resuscitator, manual, single-use
w/CO2 Detector
Ambu A/S
523611730
In Commercial Distribution

  • 05707480149629 ()
  • 05707480149612 ()
523611730

  • Pulmonary resuscitator, manual, single-use
w/CO2 Detector
Ambu A/S
523611700
In Commercial Distribution

  • 05707480149605 ()
  • 05707480149599 ()
523611700

  • Pulmonary resuscitator, manual, single-use
w/ Exhalation Filter
Ambu A/S
523611061
In Commercial Distribution

  • 05707480149582 ()
  • 05707480149575 ()

  • Adult
523611061

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
523611057
In Commercial Distribution

  • 05707480149568 ()
  • 05707480149551 ()
523611057

  • Pulmonary resuscitator, manual, single-use
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