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
523611057
In Commercial Distribution

  • 05707480149568 ()
  • 05707480149551 ()
523611057

  • Pulmonary resuscitator, manual, single-use
w/Mercury Filter
Ambu A/S
523611051
In Commercial Distribution

  • 05707480149520 ()
  • 05707480149513 ()
523611051

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
523611031
In Commercial Distribution

  • 05707480149506 ()
  • 05707480149490 ()
523611031

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
523611030
In Commercial Distribution

  • 05707480149483 ()
  • 05707480149476 ()
523611030

  • Pulmonary resuscitator, manual, single-use
w/Expiratory Filter & Manometer
Ambu A/S
523611017
In Commercial Distribution

  • 05707480149469 ()
  • 05707480149452 ()
523611017

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
523611001
In Commercial Distribution

  • 05707480149445 ()
  • 05707480149438 ()
523611001

  • Pulmonary resuscitator, manual, single-use
w/Face Mask & Manometer
Ambu A/S
523211016
In Commercial Distribution

  • 05707480149421 ()
  • 05707480149414 ()
523211016

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
521612000
In Commercial Distribution

  • 05707480149407 ()
  • 05707480149391 ()

  • Adult
521612000

  • Pulmonary resuscitator, manual, single-use
w/CO2 Detector
Ambu A/S
521611700
In Commercial Distribution

  • 05707480149384 ()
  • 05707480149377 ()
521611700

  • Pulmonary resuscitator, manual, single-use
Single Patient Use Resuscitator
Ambu A/S
521611071
In Commercial Distribution

  • 05707480149360 ()
  • 05707480149353 ()
521611071

  • Pulmonary resuscitator, manual, single-use
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