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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.
10-50808
In Commercial Distribution

  • 30641043508088 ()
  • 10641043508084 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50807
In Commercial Distribution

  • 30641043508071 ()
  • 10641043508077 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50806
In Commercial Distribution

  • 10641043508060 ()
  • 30641043508064 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50805
In Commercial Distribution

  • 10641043508053 ()
  • 30641043508057 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50804
Not in Commercial Distribution

  • 10641043508046 ()
  • 30641043508040 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50803
In Commercial Distribution

  • 10641043508039 ()
  • 30641043508033 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50802
In Commercial Distribution

  • 10641043508022 ()
  • 30641043508026 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50801
Not in Commercial Distribution

  • 10641043508015 ()
  • 30641043508019 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50800
Not in Commercial Distribution

  • 30641043508002 ()
  • 10641043508008 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-50737
In Commercial Distribution

  • 30641043507371 ()
  • 10641043507377 ()


  • Pulmonary resuscitator, manual, reusable
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