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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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C-Eye II — 3 UDI-DI variants, MDR (AssisTech Sp. z o.o.)

MD Atlas
AssisTech Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

C-Eye II

59041628300CE44

3 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: AssisTech Sp. z o.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59041628300CE44
Device name: C-Eye II
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 11, 2022

Manufacturer & authorised representative

Manufacturer

Name: AssisTech Sp. z o.o.
SRN: PL-MF-000002848
Country: Poland
Email: kontakt@assistech.eu
Phone: +48537446406

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FVM0T238F6TAVWBKPE42P0ZC

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

C-Eye05904162830008
C-Eye II05904162830015
NeuroTAB05904162830077