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 2, BTE PP 13 2.4G 105 C093
Oticon A/S
214954
In Commercial Distribution

  • 05707131379603 ()


  • Air-conduction hearing aid, behind-the-ear
RUBY 2, BTE PP 13 2.4G 105 C091
Oticon A/S
214953
In Commercial Distribution

  • 05707131379597 ()


  • Air-conduction hearing aid, behind-the-ear
RUBY 2, BTE PP 13 2.4G 105 C092
Oticon A/S
214952
In Commercial Distribution

  • 05707131379580 ()


  • Air-conduction hearing aid, behind-the-ear
RUBY 2, BTE PP 13 2.4G 105 C090
Oticon A/S
214951
In Commercial Distribution

  • 05707131379573 ()


  • Air-conduction hearing aid, behind-the-ear
RUBY 1, BTE PP 13 2.4G 105 C063
Oticon A/S
214950
In Commercial Distribution

  • 05707131379566 ()


  • Air-conduction hearing aid, behind-the-ear
RUBY 1, BTE PP 13 2.4G 105 C093
Oticon A/S
214949
In Commercial Distribution

  • 05707131379559 ()


  • Air-conduction hearing aid, behind-the-ear
RUBY 1, BTE PP 13 2.4G 105 C091
Oticon A/S
214948
In Commercial Distribution

  • 05707131379542 ()


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