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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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HI (ITE) — 46 UDI-DI variants, MDR (SBO Hearing A/S)

MD Atlas
SBO Hearing A/S

Data from EUDAMED, last updated May 31, 2026

HI (ITE)

57144640-HI-00081-RL

46 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-HI-00081-RL
Device name: —
Device model: HI (ITE)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 14, 2025

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

46 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JP9YD9SBN9V8Y966Z1YPS07S

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

25171905714464088003
25180105714464088348
25172105714464087884
25172205714464087778
25172005714464087945
25180305714464088126
25172505714464088287
25172605714464088201
25172705714464088065
25180005714464088423
25180405714464088195
25172805714464088140
25180205714464088263
25181205714464088133
25181105714464088270
25181005714464088355
25180905714464088430
26338005714464123094
26337905714464123100
26337705714464123124
26337805714464123117

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