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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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Oticon - 05707131264824

RIA, KIT 312 DIR L V BE
Oticon A/S
133853
In Commercial Distribution

  • 05707131264824 ()


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

Oticon - 05707131264817

RIA, KIT 312 DIR R V BE
Oticon A/S
133852
In Commercial Distribution

  • 05707131264817 ()


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

Oticon - 05707131264800

RIA, KIT 312 DIR L H BE
Oticon A/S
133851
In Commercial Distribution

  • 05707131264800 ()


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

Oticon - 05707131264794

RIA, KIT 312 DIR R H BE
Oticon A/S
133850
In Commercial Distribution

  • 05707131264794 ()


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

Oticon - 05707131264701

RIA PRO, KIT 312 OMNI 85 L BE
Oticon A/S
133819
In Commercial Distribution

  • 05707131264701 ()


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

Oticon - 05707131264695

RIA PRO, KIT 312 OMNI 85 R BE
Oticon A/S
133818
In Commercial Distribution

  • 05707131264695 ()


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

Oticon - 05707131264688

RIA PRO, KIT 312 DIR 85 L V BE
Oticon A/S
133817
In Commercial Distribution

  • 05707131264688 ()


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

Oticon - 05707131264671

RIA PRO, KIT 312 DIR 85 R V BE
Oticon A/S
133816
In Commercial Distribution

  • 05707131264671 ()


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

Oticon - 05707131264640

RIA PRO, KIT 312 OMNI L BE
Oticon A/S
133811
In Commercial Distribution

  • 05707131264640 ()


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

Oticon - 05707131264633

RIA PRO, KIT 312 OMNI R BE
Oticon A/S
133810
In Commercial Distribution

  • 05707131264633 ()


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