Phonak Audéo E30-R 050-1137-P4

GUDID 07613389761924

Sonova AG

Air-conduction hearing aid, receiver-in-canal
Primary Device ID07613389761924
NIH Device Record Keyc09349f9-c16a-495e-a340-53af4a0e2a3a
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhonak Audéo E30-R
Version Model Number(chestnut)
Catalog Number050-1137-P4
Company DUNS480662550
Company NameSonova AG
Device Count1
DM Exemptfalse
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107613389761924 [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 Date2026-03-25
Device Publish Date2026-03-17

On-Brand Devices [Phonak Audéo E30-R]

07613389891300(precious pink)
07613389891294(blue ocean)
07613389891287(Caribbean Blue)
07613389762006(beige)
07613389761993(atlantic green)
07613389761986(sienna red)
07613389761979(Copper)
07613389761962(velvet black)
07613389761955(graphite gray)
07613389761948(silver gray)
07613389761931(champagne)
07613389761924(chestnut)
07613389761917(sandalwood)
07613389755770(sand beige)

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.