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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.
10-50915
In Commercial Distribution

  • 30641043509153 ()
  • 10641043509159 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50914
In Commercial Distribution

  • 30641043509146 ()
  • 10641043509142 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50905
In Commercial Distribution

  • 30641043509054 ()
  • 10641043509050 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50904
In Commercial Distribution

  • 30641043509047 ()
  • 10641043509043 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50903
In Commercial Distribution

  • 30641043509030 ()
  • 10641043509036 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50902
In Commercial Distribution

  • 30641043509023 ()
  • 10641043509029 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50901
In Commercial Distribution

  • 30641043509016 ()
  • 10641043509012 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50900
In Commercial Distribution

  • 30641043509009 ()
  • 10641043509005 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50843
In Commercial Distribution

  • 30641043508439 ()
  • 10641043508435 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50842
In Commercial Distribution

  • 30641043508422 ()
  • 10641043508428 ()


  • Pulmonary resuscitator, manual, single-use
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