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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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K90, ITC/ITE AT WL R BE
Oticon A/S
109053
In Commercial Distribution

  • 05707131198624 ()


  • Air-conduction hearing aid, in-the-ear
K90, ITC/ITE AP WL L BE
Oticon A/S
109052
In Commercial Distribution

  • 05707131198617 ()


  • Air-conduction hearing aid, in-the-ear
K90, ITC/ITE AP WL R BE
Oticon A/S
109051
In Commercial Distribution

  • 05707131198600 ()


  • Air-conduction hearing aid, in-the-ear
INPR, ITE VC AT WL L BE INO PRO
Oticon A/S
109026
In Commercial Distribution

  • 05707131198570 ()


  • Air-conduction hearing aid, in-the-ear
INPR, ITE VC AT WL R BE INO PRO
Oticon A/S
109025
In Commercial Distribution

  • 05707131198563 ()


  • Air-conduction hearing aid, in-the-ear
INPR, ITE VC AP WL L BE INO PRO
Oticon A/S
109024
In Commercial Distribution

  • 05707131198556 ()


  • Air-conduction hearing aid, in-the-ear
INPR, ITE VC AP WL R BE INO PRO
Oticon A/S
109023
In Commercial Distribution

  • 05707131198549 ()


  • Air-conduction hearing aid, in-the-ear
INPR, ITC/ITE AT WL L BE INO PRO
Oticon A/S
109022
In Commercial Distribution

  • 05707131198532 ()


  • Air-conduction hearing aid, in-the-ear
INPR, ITC/ITE AT WL R BE INO PRO
Oticon A/S
109021
In Commercial Distribution

  • 05707131198525 ()


  • Air-conduction hearing aid, in-the-ear
INPR, ITC/ITE AP WL L BE INO PRO
Oticon A/S
109020
In Commercial Distribution

  • 05707131198518 ()


  • Air-conduction hearing aid, in-the-ear
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