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 RIC hearing aids — 1,371 UDI-DI variants, MDR (Sonova AG)

MD Atlas
Sonova AG

Data from EUDAMED, last updated May 23, 2026

Sonova RIC hearing aids

07613389RICWJ

1,371 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: 07613389RICWJ
Device name: Sonova RIC hearing aids
Device model: Sonova RIC hearing aids
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

1,371 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

basicUdiUlid01GM37YTGDRG1Y2F40N7Y8WYV3

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

050-0791-P307613389509724
050-0788-P107613389352566
050-0788-P707613389352603
050-0788-H007613389351514
050-0788-P807613389352610
050-0788-P507613389352580
050-0788-P307613389508086
050-0788-P607613389352597
050-0788-P407613389352573
050-0794-P107613389352207
050-0794-P607613389352238
050-0794-P507613389352221
050-0794-P407613389352214
050-0794-P707613389352245
050-0794-H007613389351576
050-0794-P807613389352252
050-0794-P307613389509762
050-0869-P607613389465426
050-0869-P107613389461466
050-0869-P407613389465419
050-0800-H007613389351637
050-0800-P507613389352016
050-0800-P407613389352009
050-0800-P707613389352030
050-0800-P107613389351996