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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.
10-51505
In Commercial Distribution

  • 30641043515055 ()
  • 10641043515051 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-51504
In Commercial Distribution

  • 30641043515048 ()
  • 10641043515044 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-51503
In Commercial Distribution

  • 30641043515031 ()
  • 10641043515037 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-51502
In Commercial Distribution

  • 30641043515024 ()
  • 10641043515020 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-51501
In Commercial Distribution

  • 30641043515017 ()
  • 10641043515013 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-51500
In Commercial Distribution

  • 30641043515000 ()
  • 10641043515006 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50916
In Commercial Distribution

  • 10641043509166 ()
  • 30641043509160 ()


  • Pulmonary resuscitator, manual, single-use
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
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