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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 Device Size Type Device Class Implantable

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No Description
MERCURY ENTERPRISES, INC.
10-55081
In Commercial Distribution

  • 30641043550810 ()
  • 10641043550816 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55080
In Commercial Distribution

  • 30641043550803 ()
  • 10641043550809 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55079
In Commercial Distribution

  • 30641043550797 ()
  • 10641043550793 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55078
In Commercial Distribution

  • 30641043550780 ()
  • 10641043550786 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55076
In Commercial Distribution

  • 30641043550766 ()
  • 10641043550762 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55074
In Commercial Distribution

  • 30641043550742 ()
  • 10641043550748 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55073
In Commercial Distribution

  • 30641043550735 ()
  • 10641043550731 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55072
In Commercial Distribution

  • 30641043550728 ()
  • 10641043550724 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55071
In Commercial Distribution

  • 30641043550711 ()
  • 10641043550717 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55070
In Commercial Distribution

  • 30641043550704 ()
  • 10641043550700 ()


  • Pulmonary resuscitator, manual, single-use
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