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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 ITE hearing aids — 247 UDI-DI variants, MDR (Sonova AG)

MD Atlas
Sonova AG

Data from EUDAMED, last updated May 23, 2026

Sonova ITE hearing aids

07613389ITEWA

247 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

247 UDI-DI variants

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Applied filters

basicUdiUlid01GM3GE4J8NJCAYWMDR75YP9S1

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

063-6397-015007613389814873
063-6392-015007613389814828
063-6398-015007613389814880
063-6393-015007613389814835
063-6399-015007613389814897
063-6394-015007613389814842
063-6400-015007613389814903
063-6395-015007613389814859
063-6401-015007613389814910
063-6396-015007613389814866
063-0519-0107613389504712
063-0523-0107613389504750
063-0518-0107613389503401
063-0522-0107613389504743
063-0517-0107613389503395
063-0521-0107613389504736
063-0525-0107613389522334
063-0516-0107613389503388
063-0520-0107613389504729
063-0524-0107613389522327
063-6397-016507613389814477
063-6392-016507613389814705
063-6398-016507613389814484
063-6393-016507613389814712
063-6399-016507613389814491

1 2 3 4 5

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 07613389ITEWA
Device name: Sonova ITE hearing aids
Device model: Sonova ITE hearing aids
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 13, 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