Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

ITE KIT Family — 94 UDI-DI variants, MDR (Ear-Technic GmbH)

MD Atlas
Ear-Technic GmbH

Data from EUDAMED, last updated May 23, 2026

ITE KIT Family

426245117ITE283

94 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426245117ITE283
Device name: ITE KIT Family
Device model: ITEKIT 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

94 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KNP0JF0HG6Y9ETVMEHGE66JJ

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

161D01 - 0702015104262451171074
141D01-0236010304262451171296
160D01 - 0701011004262451170817
160D01 - 0701010304262451170794
134D01-0234016404262451171197
160D01 - 0701011204262451170831
133D01-0233019204262451171128
161D01 - 0702014504262451171012
161D01 - 0702013704262451170930
161D01 - 0702013904262451170954
160D01 - 0701011904262451170855
161D01 - 0702013804262451170947
133D01-0233019604262451171142
142D01-0235016404262451171258
161D01 - 0702014104262451170978
133D01-0233016404262451171135
161D01 - 0702014304262451170992
134D01-0234019204262451171180
160D01 - 0701012904262451170909

1 2 3 4