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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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CardioSignal — 4 UDI-DI variants, MDR (Precordior Oy)

MD Atlas
Precordior Oy

Data from EUDAMED, last updated May 23, 2026

CardioSignal

643008145CSAFIB3Y

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Precordior Oy

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Device characteristics

Active deviceMeasuring function

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 643008145CSAFIB3Y
Device name: CardioSignal
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Nov 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Precordior Oy
SRN: FI-MF-000014540
Country: Finland
Email: support@cardiosignal.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K9EPZX0V27HH8MF6PKW7GGW3

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

iOS v. 3.106430081450052
Android v. 3.106430081450069
iOS v. 1.006430081450076
Android v. 1.006430081450083