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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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UNEEG EpiSight Analyzer — 3 UDI-DI variants, MDR

MD Atlas
AIT Austrian Institute of Technology GmbH

Data from EUDAMED, last updated May 23, 2026

UNEEG EpiSight Analyzer

912010983EPISIGHT2AF

3 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: AIT Austrian Institute of Technology GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 912010983EPISIGHT2AF
Device name: UNEEG EpiSight Analyzer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Jan 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: AIT Austrian Institute of Technology GmbH
SRN: AT-MF-000002398
Country: Austria
Email: office@ait.ac.at
Phone: +43 50 550 - 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GQ1Z3VTX7QG8QRCB19S0B6GD

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

UNEEG EpiSight Analyzer 2.009120109830115
UNEEG™ EpiSight Analyzer09120109830276
UNEEG™ EpiSight Analyzer 2.109120109830177