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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.
10-56004
In Commercial Distribution

  • 30641043560048 ()
  • 10641043560044 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56003
In Commercial Distribution

  • 30641043560031 ()
  • 10641043560037 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56002
In Commercial Distribution

  • 30641043560024 ()
  • 10641043560020 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56001
In Commercial Distribution

  • 30641043560017 ()
  • 10641043560013 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55931
In Commercial Distribution

  • 30641043559318 ()
  • 10641043559314 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55930
In Commercial Distribution

  • 30641043559301 ()
  • 10641043559307 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55928
In Commercial Distribution

  • 30641043559288 ()
  • 10641043559284 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55924
In Commercial Distribution

  • 30641043559240 ()
  • 10641043559246 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55923
In Commercial Distribution

  • 30641043559233 ()
  • 10641043559239 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-55922
In Commercial Distribution

  • 30641043559226 ()
  • 10641043559222 ()


  • Pulmonary resuscitator, manual, single-use
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