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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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Patient cable for Walk400h — 3 UDI-DI variants, MDR (CARDIOLINE SpA)

MD Atlas
CARDIOLINE SpA

Data from EUDAMED, last updated May 31, 2026

Patient cable for Walk400h

08056732650230000168

3 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: CARDIOLINE SpA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 08056732650230000168
Device name: Patient cable for Walk400h
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: CARDIOLINE SpA
SRN: IT-MF-000029682
Country: Italy
Email: compliance@cardioline.com
Phone: +39046196821

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K1X1QN9K1776VCJA2CH8PJ5W

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

6305010108056732652705
6305010008056732652682
6305009908056732652675