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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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Multi-Link™ Single-Patient-Use ECG… — 28 UDI-DI variants, MDR

MD Atlas
AirLife Finland Oy

Data from EUDAMED, last updated May 23, 2026

Multi-Link™ Single-Patient-Use ECG Leadwire Set

0190752TDHEL1311UP

28 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: AirLife Finland Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0190752TDHEL1311UP
Device name: Multi-Link™ Single-Patient-Use ECG Leadwire Set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 17, 2021

Manufacturer & authorised representative

Manufacturer

Name: AirLife Finland Oy
SRN: FI-MF-000001482
Country: Finland
Email: jsillanpaa@myairlife.com

Variants by status

UDI-DI variants

28 UDI-DI variants

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basicUdiUlid01FQ3GH8EA85DP9HNW53VYRF5G

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

Multi-Link™ Single-Patient-Use ECG Leadwire Set C-LEAD, SNAP, IEC, 100 cm/39 in10190752179424
Multi-Link™ Single-Patient-Use ECG Leadwire Set V-LEAD, GRABBER, AHA, 100 cm/39 in10190752179578
Multi-Link™ Single-Patient-Use ECG Leadwire Set V-LEAD, SNAP, AHA, 100 cm/39 in10190752179462

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