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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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Patient cable cleared with H12+ recorder
MORTARA INSTRUMENT, INC.
9293-028-50
In Commercial Distribution

  • 00812345023060 ()


  • Electrocardiographic lead set, reusable
Cable cleared with Q-Stress Stress Exercise System
MORTARA INSTRUMENT, INC.
60-00185-01
In Commercial Distribution

  • 00812345023046 ()


  • Electrocardiographic lead set, reusable
Cable cleared with Q-Stress Stress Exercise System
MORTARA INSTRUMENT, INC.
60-00181-01
In Commercial Distribution

  • 00812345023022 ()


  • Electrocardiographic lead set, reusable
Patient cable cleared with X12+
MORTARA INSTRUMENT, INC.
9293-034-50
In Commercial Distribution

  • 00812345023015 ()


  • Electrocardiographic lead set, reusable
Cable cleared with Q-Stress Stress Exercise System
MORTARA INSTRUMENT, INC.
60-00184-01
In Commercial Distribution

  • 00812345022858 ()


  • Electrocardiographic lead set, reusable
Cable cleared with Q-Stress Stress Exercise System
MORTARA INSTRUMENT, INC.
60-00180-01
In Commercial Distribution

  • 00812345022834 ()


  • Electrocardiographic lead set, reusable
Patient cable cleared with XScribe Stress System
MORTARA INSTRUMENT, INC.
9293-047-70
In Commercial Distribution

  • 00812345022766 ()


  • Electrocardiographic lead set, reusable
Patient cable cleared with H12+/X12+
MORTARA INSTRUMENT, INC.
9293-026-50
In Commercial Distribution

  • 00812345022728 ()


  • Electrocardiographic lead set, reusable
Patient cable cleared with H12+/X12+
MORTARA INSTRUMENT, INC.
9293-017-50
In Commercial Distribution

  • 00812345022711 ()


  • Electrocardiographic lead set, reusable
Patient cable cleared with ELI 380
MORTARA INSTRUMENT, INC.
9293-047-66
In Commercial Distribution

  • 00812345022025 ()


  • Electrocardiographic lead set, reusable
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