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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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GN ReSound - 05708296202768

HI,KE498-DW,STRL GRY
Gn Hearing A/S
21497420
In Commercial Distribution

  • 05708296202768 ()


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

GN ReSound - 05708296202751

HI,KE498-DW,BLK
Gn Hearing A/S
21497408
In Commercial Distribution

  • 05708296202751 ()


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

GN ReSound - 05708296202744

HI,KE498-DW,BGE
Gn Hearing A/S
21497405
In Commercial Distribution

  • 05708296202744 ()


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

GN ReSound - 05708296202737

HI,KE498-DW,DBR
Gn Hearing A/S
21497404
In Commercial Distribution

  • 05708296202737 ()


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

GN ReSound - 05708296202720

HI,KE498-DW,MBL
Gn Hearing A/S
21497402
In Commercial Distribution

  • 05708296202720 ()


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

GN ReSound - 05708296202713

HI,KE288-DWH,STRL GRY
Gn Hearing A/S
21497320
In Commercial Distribution

  • 05708296202713 ()


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

GN ReSound - 05708296202706

HI,KE288-DWH,BLK
Gn Hearing A/S
21497308
In Commercial Distribution

  • 05708296202706 ()


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

GN ReSound - 05708296202690

HI,KE288-DWH,BGE
Gn Hearing A/S
21497305
In Commercial Distribution

  • 05708296202690 ()


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

GN ReSound - 05708296202683

HI,KE288-DWH,DBR
Gn Hearing A/S
21497304
In Commercial Distribution

  • 05708296202683 ()


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

GN ReSound - 05708296202676

HI,KE288-DWH,MBL
Gn Hearing A/S
21497302
In Commercial Distribution

  • 05708296202676 ()


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