Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Sonova BTE hearing aids — 1,215 UDI-DI variants, MDR (Sonova AG)

MD Atlas
Sonova AG

Data from EUDAMED, last updated May 23, 2026

Sonova BTE hearing aids

07613389BTEV7

1,215 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Sonova AG

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 07613389BTEV7
Device name: Sonova BTE hearing aids
Device model: Sonova BTE hearing aids
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: Sonova AG
SRN: CH-MF-000015958
Country: Switzerland
Email: CH-PH-OPS-RA@sonova.com

Authorised representative

Name: Sonova Deutschland GmbH
SRN: DE-AR-000006322
Country: Germany
Phone: +49 711 51070 0

Variants by status

UDI-DI variants

1,215 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01H8BWVZSXYK6HQ6DJ2DETGJWJ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

050-6827-P77207613389681055
050-6827-P67207613389681017
050-6827-R87207613389681086
050-6862-P47207613389750898
050-6862-P77207613389750515
050-6862-P67207613389750249
050-6862-R87207613389750751
050-6828-P47207613389681109
050-6828-P77207613389681161
050-6828-P67207613389681130
050-6828-R87207613389681192
050-6863-P47207613389750904
050-6863-P67207613389750270
050-6829-P47207613389681208
050-6829-P77207613389681284
050-6829-P67207613389681246
050-6829-R87207613389681314
050-6830-P47207613389681338
050-6830-P77207613389681413
050-6830-P67207613389681376
050-6830-R87207613389681444
050-6901-P75807613389739459
050-6901-P65807613389739442
050-6901-R85807613389739466
050-6902-P75807613389739480