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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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Preventicus Heartbeats & Preventicus… — 5 UDI-DI variants, MDR

MD Atlas
Preventicus GmbH

Data from EUDAMED, last updated May 23, 2026

Preventicus Heartbeats & Preventicus Nightwatch

409996600000GK

5 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: Preventicus GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 409996600000GK
Device name: Preventicus Heartbeats & Preventicus Nightwatch
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: Jun 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Preventicus GmbH
SRN: DE-MF-000008931
Country: Germany
Email: info@preventicus.com
Phone: +49 3641 5598450

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

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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

Preventicus Heartbeats App04099966000182
Preventicus Heartbeats App04099966000175
Preventicus Heartbeats Core04099966000212
Preventicus Nightwatch04099966000106
Preventicus Nightwatch04099966000113