eudamed_udi Primary ID: 10190752182288

Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set 5-Lead Set, Grabber, IEC, 3.6 m/12 ft (UDI 10190752182288)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set 5-Lead Set, Grabber, IEC, 3.6 m/12 ft (Model/Catalog Number: 2052133-402) is a medical device manufactured by AirLife Finland Oy. This product is indexed under FDA Product Code / Category Classification Z12050385 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2052133-402
Product Code / EMDN: Z12050385
Device Name: Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set
Database Sync Date: 2026-08-09 16:46:55

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set 5-Lead Set, Grabber, IEC, 3.6 m/12 ft?

The registered manufacturer of record for Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set 5-Lead Set, Grabber, IEC, 3.6 m/12 ft is AirLife Finland Oy.

What is the Primary UDI-DI identifier for Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set 5-Lead Set, Grabber, IEC, 3.6 m/12 ft?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10190752182288.

What classification code is assigned to this device?

This device is registered under product classification code Z12050385.

Similar Classification Devices (Z12050385)

Other Devices by AirLife Finland Oy

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