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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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Fitting Software — 12 UDI-DI variants, MDR (SBO Hearing A/S)

MD Atlas
SBO Hearing A/S

Data from EUDAMED, last updated May 23, 2026

Fitting Software

57144640-fSW-000012-28

12 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: SBO Hearing A/S

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 57144640-fSW-000012-28
Device name: —
Device model: Fitting Software
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Aug 1, 2024

Manufacturer & authorised representative

Manufacturer

Name: SBO Hearing A/S
SRN: DK-MF-000001270
Country: Denmark
Email: info@demant.com
Phone: +45 3917 7100

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01J470YNY1K3T6K6CSS3HMK709

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

26287305714464122516
26833605714464131914
27048805714464139422
27490805714464146239
27490905714464146246
28606605714464175413
28503105714464167692
28503005714464167685
27048705714464139415
28606505714464175406
26833705714464131921
26287205714464122509