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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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ZR3, KIT 312 NFM 75 L BE ZERENA 3
Bernafon AG
192007
In Commercial Distribution

  • 05711584086810 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 NFM 75 R BE ZERENA 3
Bernafon AG
192006
In Commercial Distribution

  • 05711584086803 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 2.4G NFM PB L BE ZERENA 3
Bernafon AG
192005
In Commercial Distribution

  • 05711584086797 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 2.4G NFM PB R BE ZERENA 3
Bernafon AG
192004
In Commercial Distribution

  • 05711584086780 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 2.4G NFM L BE ZERENA 3
Bernafon AG
192003
In Commercial Distribution

  • 05711584086773 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 2.4G NFM R BE ZERENA 3
Bernafon AG
192002
In Commercial Distribution

  • 05711584086766 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 2.4G NFM 90 PB L BE ZERENA 3
Bernafon AG
192001
In Commercial Distribution

  • 05711584086759 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 2.4G NFM 90 PB R BE ZERENA 3
Bernafon AG
192000
In Commercial Distribution

  • 05711584086742 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 2.4G NFM 90 L BE ZERENA 3
Bernafon AG
191999
In Commercial Distribution

  • 05711584086735 ()


  • Air-conduction hearing aid, in-the-ear
ZR3, KIT 312 2.4G NFM 90 R BE ZERENA 3
Bernafon AG
191998
In Commercial Distribution

  • 05711584086728 ()


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