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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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n/a - 04961333231515

CD, 3506 VERSION 3.3, REV.D
PENTAX OF AMERICA, INC.
7188-0100
In Commercial Distribution

  • 04961333231515 ()


  • Electroglottograph

n/a - 04961333231508

CD, 5104 VERSION 3.2,REV.C
PENTAX OF AMERICA, INC.
7187-9900
In Commercial Distribution

  • 04961333231508 ()


  • Electroglottograph

n/a - 04961333231492

CD, 4337 VERSION 3.2,REV.C
PENTAX OF AMERICA, INC.
7187-9000
In Commercial Distribution

  • 04961333231492 ()


  • Electroglottograph

n/a - 04961333231485

CD, 5150 VERSION 3.4.1,REV.D
PENTAX OF AMERICA, INC.
7187-8900
In Commercial Distribution

  • 04961333231485 ()


  • Electroglottograph

n/a - 04961333231478

CD, 5138 VERSION 3.3, REV.D
PENTAX OF AMERICA, INC.
7187-8800
In Commercial Distribution

  • 04961333231478 ()


  • Electroglottograph

n/a - 04961333231461

CD, 4332 VERSION 3.2,REV.C
PENTAX OF AMERICA, INC.
7187-8600
In Commercial Distribution

  • 04961333231461 ()


  • Electroglottograph

n/a - 04961333231454

CD, 5141 VERSION 3.3, REV.D
PENTAX OF AMERICA, INC.
7187-8000
In Commercial Distribution

  • 04961333231454 ()


  • Electroglottograph

n/a - 04961333231447

CD, 5129 VERSION 3.3, REV.D
PENTAX OF AMERICA, INC.
7187-7800
In Commercial Distribution

  • 04961333231447 ()


  • Electroglottograph

n/a - 04961333231430

CD, 5127 VERSION 3.3, REV.D
PENTAX OF AMERICA, INC.
7187-7700
In Commercial Distribution

  • 04961333231430 ()


  • Electroglottograph

n/a - 04961333231423

CD, 5121 VERSION 3.3, REV.D
PENTAX OF AMERICA, INC.
7187-7600
In Commercial Distribution

  • 04961333231423 ()


  • Electroglottograph
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