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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Single Patient Use Resuscitator
Ambu A/S
520200000
In Commercial Distribution

  • 05707480151547 ()
  • 05707480151530 ()

  • Adult
520200000

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
530214000B
In Commercial Distribution

  • 05707480151523 ()
  • 05707480151516 ()

  • Pediatric
530214000B

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
544216069
In Commercial Distribution

  • 05707480151424 ()
  • 05707480151417 ()
544216069

  • Pulmonary resuscitator, manual, single-use
w/Manometer & CO2 Detector
Ambu A/S
544212830
In Commercial Distribution

  • 05707480151363 ()
  • 05707480151356 ()
544212830

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
544212017
In Commercial Distribution

  • 05707480151264 ()
  • 05707480151257 ()
544212017

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
540212010
In Commercial Distribution

  • 05707480151004 ()
  • 05707480150991 ()

  • Infant
540212010

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
531613047
In Commercial Distribution

  • 05707480150762 ()
  • 05707480150755 ()
531613047

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
531613031
In Commercial Distribution

  • 05707480150724 ()
  • 05707480150717 ()
531613031

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
531613030
In Commercial Distribution

  • 05707480150700 ()
  • 05707480150694 ()
531613030

  • Pulmonary resuscitator, manual, single-use
with Filter
Ambu A/S
531613017
In Commercial Distribution

  • 05707480150687 ()
  • 05707480150670 ()
531613017

  • Pulmonary resuscitator, manual, single-use
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