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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ENDOPRO IQ REVIEW LICENSE (20-30)
PENTAX OF AMERICA, INC.
M70218-UP
In Commercial Distribution

  • 04961333243730 ()
  • 14961333243737 ()


  • Radiology information system
ENDOPRO IQ REVIEW LICENSE (20-30)
PENTAX OF AMERICA, INC.
M70218
In Commercial Distribution

  • 04961333243723 ()
  • 14961333243720 ()


  • Radiology information system
ENDOPRO IQ REVIEW LICENSE (10-19)
PENTAX OF AMERICA, INC.
M70217-UP
In Commercial Distribution

  • 04961333243716 ()
  • 14961333243713 ()


  • Radiology information system
ENDOPRO IQ REVIEW LICENSE (10-19)
PENTAX OF AMERICA, INC.
M70217
In Commercial Distribution

  • 04961333243709 ()
  • 14961333243706 ()


  • Radiology information system
ENDOPRO IQ REVIEW LICENSE (1-4)
PENTAX OF AMERICA, INC.
M70216-UP
In Commercial Distribution

  • 04961333243693 ()
  • 14961333243690 ()


  • Radiology information system
ENDOPRO IQ REVIEW LICENSE (1-4)
PENTAX OF AMERICA, INC.
M70216
In Commercial Distribution

  • 04961333243686 ()
  • 14961333243683 ()


  • Radiology information system
NURSING NOTES
PENTAX OF AMERICA, INC.
M70214-UP
In Commercial Distribution

  • 04961333243679 ()


  • Radiology information system
NURSING NOTES
PENTAX OF AMERICA, INC.
M70214
In Commercial Distribution

  • 04961333243662 ()


  • Radiology information system
DOC-U-SCRIBE REPORTING
PENTAX OF AMERICA, INC.
M70213-UP
In Commercial Distribution

  • 04961333243655 ()


  • Radiology information system
DOC-U-SCRIBE REPORTING
PENTAX OF AMERICA, INC.
M70213
In Commercial Distribution

  • 04961333243648 ()


  • Radiology information system
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