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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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heartfish App — 2 UDI-DI variants, MDR (heartfish GmbH)

MD Atlas
heartfish GmbH

Data from EUDAMED, last updated May 23, 2026

heartfish App

9120124580001SH

2 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: heartfish GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 9120124580001SH
Device name: heartfish App
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Aug 18, 2022

Manufacturer & authorised representative

Manufacturer

Name: heartfish GmbH
SRN: AT-MF-000018123
Country: Austria
Email: office@heartfish.io

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GARBR8R894ZCA4W57B9YN1K3

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

1.0.009120124580026
1.0.009120124580019