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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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HA INTUIS SP 4.1 DKC
Ws Audiology Usa, Inc.
Intuis SP 4.1
In Commercial Distribution

  • 05714880183139 ()
21015047

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.1 DBR
Ws Audiology Usa, Inc.
Intuis SP 4.1
In Commercial Distribution

  • 05714880183122 ()
21015044

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.1 BLK
Ws Audiology Usa, Inc.
Intuis SP 4.1
In Commercial Distribution

  • 05714880183115 ()
21015042

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.1 BG
Ws Audiology Usa, Inc.
Intuis SP 4.1
In Commercial Distribution

  • 05714880183108 ()
21015040

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.0 SLH
Ws Audiology Usa, Inc.
Intuis SP 4.0
In Commercial Distribution

  • 05714880182996 ()
21015091

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.0 SB
Ws Audiology Usa, Inc.
Intuis SP 4.0
In Commercial Distribution

  • 05714880182989 ()
21015089

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.0 RGD
Ws Audiology Usa, Inc.
Intuis SP 4.0
In Commercial Distribution

  • 05714880182972 ()
21015087

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.0 PRL
Ws Audiology Usa, Inc.
Intuis SP 4.0
In Commercial Distribution

  • 05714880182965 ()
21015085

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.0 GPH
Ws Audiology Usa, Inc.
Intuis SP 4.0
In Commercial Distribution

  • 05714880182958 ()
21015083

  • Air-conduction hearing aid, behind-the-ear
HA INTUIS SP 4.0 DKC
Ws Audiology Usa, Inc.
Intuis SP 4.0
In Commercial Distribution

  • 05714880182941 ()
21015079

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