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

050-6455-UC07613389492682
050-6455-UB07613389492675
050-6455-U407613389481785
050-6456-U607613389492699
050-6456-UA07613389492705
050-6456-UC07613389492729
050-6456-UB07613389492712
050-6456-U407613389481792
050-6457-U607613389492736
050-6457-UA07613389492743
050-6457-UC07613389492767
050-6457-UB07613389492750
050-6457-U407613389481808
050-6458-U607613389492774
050-6458-UA07613389492781
050-6458-UC07613389492804
050-6458-UB07613389492798
050-6458-U407613389481815
050-6459-U407613389481822
050-6831-P67507613389657999
050-6827-P77507613389767421
050-6827-P67507613389767285
050-6827-R87507613389767438
050-6828-P77507613389767445
050-6828-P67507613389767292