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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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SeeTech Only — 5 UDI-DI variants, MDR (Humanelektronik GmbH)

MD Atlas
Humanelektronik GmbH

Data from EUDAMED, last updated May 23, 2026

SeeTech Only

426076432HESeeTech6C

5 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: 426076432HESeeTech6C
Device name: SeeTech Only
Device model: Augensteuerung SeeTech
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 15, 2023

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

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H8JZVBGRZSZQ2RY098BTR6Z3

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

10021041s04260764320158
95404260764320172
40210504260764320165
266904260764320141
1002104404260764320011