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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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DeepRhythmAI — 1 UDI-DI variant, MDR (Medicalgorithmics S.A.)

MD Atlas
Medicalgorithmics S.A.

Data from EUDAMED, last updated May 30, 2026

DeepRhythmAI

590302156DRAI23K

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: Medicalgorithmics S.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 590302156DRAI23K
Device name: DeepRhythmAI
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: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medicalgorithmics S.A.
SRN: PL-MF-000011413
Country: Poland
Email: regulatory@medicalgorithmics.com
Phone: +48 22 825 12 49

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KR3W3QHGZWQA9F1Y3TDD5VZ6

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

DeepRhythmAI05903021560834