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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RUBY 1, BTE PP 13 2.4G 105 C092
Oticon A/S
214947
In Commercial Distribution

  • 05707131379535 ()


  • Air-conduction hearing aid, behind-the-ear
RUBY 1, BTE PP 13 2.4G 105 C090
Oticon A/S
214946
In Commercial Distribution

  • 05707131379528 ()


  • Air-conduction hearing aid, behind-the-ear
G10, BTE 13 PP 2.4G 105 C063 REVEAL
Oticon A/S
193404
In Commercial Distribution

  • 05707131342072 ()


  • Air-conduction hearing aid, behind-the-ear
G10, BTE 13 PP 2.4G 105 C093 REVEAL
Oticon A/S
193403
In Commercial Distribution

  • 05707131342065 ()


  • Air-conduction hearing aid, behind-the-ear
G10, BTE 13 PP 2.4G 105 C091 REVEAL
Oticon A/S
193402
In Commercial Distribution

  • 05707131342058 ()


  • Air-conduction hearing aid, behind-the-ear
G10, BTE 13 PP 2.4G 105 C092 REVEAL
Oticon A/S
193401
In Commercial Distribution

  • 05707131342041 ()


  • Air-conduction hearing aid, behind-the-ear
G10, BTE 13 PP 2.4G 105 C090 REVEAL
Oticon A/S
193400
In Commercial Distribution

  • 05707131342034 ()


  • Air-conduction hearing aid, behind-the-ear
G10, BTE 13 PP 2.4G 105 C063 EARQ
Oticon A/S
193383
In Commercial Distribution

  • 05707131342027 ()


  • Air-conduction hearing aid, behind-the-ear
G10, BTE 13 PP 2.4G 105 C093 EARQ
Oticon A/S
193382
In Commercial Distribution

  • 05707131342010 ()


  • Air-conduction hearing aid, behind-the-ear
G10, BTE 13 PP 2.4G 105 C091 EARQ
Oticon A/S
193381
In Commercial Distribution

  • 05707131342003 ()


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