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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 Focus device — 11 UDI-DI variants, MDR (Sonova AG)

MD Atlas
Sonova AG

Data from EUDAMED, last updated May 23, 2026

Sonova Focus device

07613389FOCUSKU

11 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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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 07613389FOCUSKU
Device name: Sonova Focus device
Device model: Sonova Focus device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 18, 2026

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

11 UDI-DI variants

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Applied filters

basicUdiUlid01KHR8KWJWMHHJH9TS1YGJN58M

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

Roger Focus II (caribbean pirate)07613389275513
056-3006-Q207613389275506
056-3006-M807613389275445
056-3006-T307613389275520
056-3006-P807613389275490
056-3006-H007613389275414
056-3006-M707613389275438
056-3006-P607613389275483
056-3005-P807613389275674
056-3005-P607613389274165
056-3006-M607613389275421