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

050-6876-U607613389736397
050-6876-UA07613389736403
050-6876-UC07613389736427
050-6876-UB07613389736410
050-6876-U407613389735857
050-6852-U607613389656213
050-6852-UA07613389656220
050-6852-UC07613389656244
050-6852-UB07613389656237
050-6852-U407613389654714
050-6883-U607613389736632
050-6883-UA07613389736649
050-6883-UC07613389736663
050-6883-UB07613389736656
050-6883-U407613389735925
050-6877-U607613389736434
050-6877-UA07613389736441
050-6877-UC07613389736465
050-6877-UB07613389736458
050-6877-U407613389735864
050-6853-U607613389656251
050-6853-UA07613389656268
050-6853-UC07613389656282
050-6853-UB07613389656275
050-6853-U407613389654721