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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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HeartScreen ECG — 2 UDI-DI variants, MDR

MD Atlas
Innomed Medical Orvostechnikai Fejlesztő és Gyártó zártkörűen működő részvénytársaság

Data from EUDAMED, last updated May 24, 2026

HeartScreen ECG

599957457HSC32

2 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: Innomed Medical Orvostechnikai Fejlesztő és Gyártó zártkörűen működő részvénytársaság

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 599957457HSC32
Device name: HeartScreen ECG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: Innomed Medical Orvostechnikai Fejlesztő és Gyártó zártkörűen működő részvénytársaság
SRN: HU-MF-000017747
Country: Hungary
Email: kovacs.pal@innomed.hu
Phone: +36301534089

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KF3AA2EHJYG0PMKF1RR3RVYJ

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

HS112C-105999574570055
HS80G-L105999574570154