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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.
10-54202
In Commercial Distribution

  • 30641043542020 ()
  • 10641043542026 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-54201
In Commercial Distribution

  • 30641043542013 ()
  • 10641043542019 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-54200
In Commercial Distribution

  • 10641043542002 ()
  • 30641043542006 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-54112
In Commercial Distribution

  • 30641043541122 ()
  • 10641043541128 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-54111
In Commercial Distribution

  • 30641043541115 ()
  • 10641043541111 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-54108
In Commercial Distribution

  • 30641043541085 ()
  • 10641043541081 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-54103
In Commercial Distribution

  • 30641043541030 ()
  • 10641043541036 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-54102
In Commercial Distribution

  • 30641043541023 ()
  • 10641043541029 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-54100
In Commercial Distribution

  • 30641043541009 ()
  • 10641043541005 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-51506
In Commercial Distribution

  • 30641043515062 ()
  • 10641043515068 ()


  • Pulmonary resuscitator, manual, single-use
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