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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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ITE Family — 30 UDI-DI variants, MDR (Ear-Technic GmbH)

MD Atlas
Ear-Technic GmbH

Data from EUDAMED, last updated May 23, 2026

ITE Family

426245117ITE17Z

30 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: Ear-Technic GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426245117ITE17Z
Device name: ITE Family
Device model: ITE Hearing Aids Series
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ear-Technic GmbH
SRN: DE-MF-000043916
Country: Germany
Email: yagmur.renkveren@eartechnic.com
Phone: +49 421 66598923

Variants by status

UDI-DI variants

30 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNPHW540AHAKPQEHCKCNZEM9

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

134D01-0234017104262451171159
161D01 - 0702014804262451171043
171D01 - 0804011004262451172514
133D01-0233017104262451171098
161D01 - 0702014404262451171005

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