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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.
10-58603
In Commercial Distribution

  • 30641043586031 ()
  • 10641043586037 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58600
In Commercial Distribution

  • 30641043586000 ()
  • 10641043586006 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58514
In Commercial Distribution

  • 30641043585140 ()
  • 10641043585146 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58512
In Commercial Distribution

  • 30641043585126 ()
  • 10641043585122 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58509
In Commercial Distribution

  • 30641043585096 ()
  • 10641043585092 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58507
In Commercial Distribution

  • 30641043585072 ()
  • 10641043585078 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58506
In Commercial Distribution

  • 30641043585065 ()
  • 10641043585061 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58503
In Commercial Distribution

  • 30641043585034 ()
  • 10641043585030 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58502
In Commercial Distribution

  • 30641043585027 ()
  • 10641043585023 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-58501
In Commercial Distribution

  • 30641043585010 ()
  • 10641043585016 ()


  • Pulmonary resuscitator, manual, single-use
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