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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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EcgViewer Light — 1 UDI-DI variant, MDR (drEryk sp. z o.o.)

MD Atlas
drEryk sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

EcgViewer Light

59052741810EcgViewerCU

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: drEryk sp. z o.o.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 59052741810EcgViewerCU
Device name: EcgViewer Light
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: Nov 14, 2022

Manufacturer & authorised representative

Manufacturer

Name: drEryk sp. z o.o.
SRN: PL-MF-000025097
Country: Poland
Email: biuro@dreryk.pl
Phone: +48 12 380 08 84

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01GHVRC82DPSKXQT2046VXPJE7

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

3.005905274181019