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

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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

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UDI-DI variants

1,215 UDI-DI variants

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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

050-6436-P44407613389473247
050-6436-P74407613389473261
050-6436-P64407613389473254
050-6436-R84407613389473278
050-6441-P44407613389471502
050-6441-P74407613389476323
050-6441-P64407613389476316
050-6441-R84407613389476330
050-6437-P44407613389473285
050-6437-P74407613389473308
050-6437-P64407613389473292
050-6437-R84407613389474312
050-6442-P44407613389476347
050-6442-P74407613389476361
050-6442-P64407613389476354
050-6442-R84407613389476378
050-6438-P44407613389474329
050-6438-P74407613389474343
050-6438-P64407613389474336
050-6438-R84407613389474350
050-6443-P44407613389476385
050-6443-P74407613389476408
050-6443-P64407613389476392
050-6443-R84407613389476415
050-6439-P44407613389474367

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