Au A-UP 050-6903-R874

GUDID 07613389799712

Sonova AG

Air-conduction hearing aid, behind-the-ear
Primary Device ID07613389799712
NIH Device Record Key5c0e193d-ce94-4155-a5d5-256d4e53ac5c
Commercial Distribution StatusIn Commercial Distribution
Brand NameAu A-UP
Version Model Numbersand
Catalog Number050-6903-R874
Company DUNS480662550
Company NameSonova AG
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com
Phone0589280101
Emailinfo@sonova.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107613389799712 [Primary]

FDA Product Code

OSMHearing Aid, Air-Conduction With Wireless Technology, Prescription

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-04-01
Device Publish Date2025-03-24

On-Brand Devices [Au A-UP]

07613389799712sand
07613389799378pewter
07613389799033espresso
07613389798340platinum

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.