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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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HE PROEye — 4 UDI-DI variants, MDR (Humanelektronik GmbH)

MD Atlas
Humanelektronik GmbH

Data from EUDAMED, last updated May 23, 2026

HE PROEye

426076432HEPROEye47

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Humanelektronik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426076432HEPROEye47
Device name: HE PROEye
Device model: HE Kommunikator PROEye
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 9, 2024

Manufacturer & authorised representative

Manufacturer

Name: Humanelektronik GmbH
SRN: DE-MF-000013990
Country: Germany
Email: info@humanelektronik.de
Phone: +49624149691-0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J9RKV7TQJASTEZX6S7Y5SF9Y

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

215904260764320370
154004260764320349
207004260764320356
164604260764320363