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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.
10-56839
In Commercial Distribution

  • 30641043568396 ()
  • 10641043568392 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56838
In Commercial Distribution

  • 30641043568389 ()
  • 10641043568385 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56837
In Commercial Distribution

  • 30641043568372 ()
  • 10641043568378 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56836
In Commercial Distribution

  • 30641043568365 ()
  • 10641043568361 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56835
In Commercial Distribution

  • 30641043568358 ()
  • 10641043568354 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56834
In Commercial Distribution

  • 30641043568341 ()
  • 10641043568347 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56833
In Commercial Distribution

  • 30641043568334 ()
  • 10641043568330 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56832
In Commercial Distribution

  • 30641043568327 ()
  • 10641043568323 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56831
In Commercial Distribution

  • 30641043568310 ()
  • 10641043568316 ()


  • Pulmonary resuscitator, manual, single-use
No Description
MERCURY ENTERPRISES, INC.
10-56830
In Commercial Distribution

  • 30641043568303 ()
  • 10641043568309 ()


  • Pulmonary resuscitator, manual, single-use
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