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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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Wireless CI receiver — 9 UDI-DI variants, MDR (Sonova AG)

MD Atlas
Sonova AG

Data from EUDAMED, last updated May 23, 2026

Wireless CI receiver

07613389WCIRQF

9 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

Active device

Identity & classification

Basic UDI-DI: 07613389WCIRQF
Device name: Wireless CI receiver
Device model: Wireless CI receiver
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 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

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01HA7D6E4YG36RNBQX2Z3NXHDV

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

056-3001-P907613389073102
056-3001-P607613389073089
056-3001-P807613389073096
056-3001-Q107613389073119
056-3001-T707613389073133
056-3001-P1 07613389069723
056-3001-P407613389073072
056-3001-XP07613389073140
056-3001-Q307613389073126