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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 in ear hearing solution… — 7 UDI-DI variants, MDR (Sonova AG)

MD Atlas
Sonova AG

Data from EUDAMED, last updated May 23, 2026

Sonova in ear hearing solution assistant tools

07613389IAHSATH8

7 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 07613389IAHSATH8
Device name: Sonova in ear hearing solution assistant tools
Device model: Sonova in ear hearing solution assistant tools
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 15, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01H9JSRDW92X5JMGWRRWWKNX9M

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

054-076707613275561577
054-076807613275561584
054-076907613275561591
054-095207613389392647
058-015107613389392746
054-095307613389392654
054-084707613389131406