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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 13 wires for HD+ — 12 UDI-DI variants, MDR

MD Atlas
CARDIOLINE SpA

Data from EUDAMED, last updated May 31, 2026

Patient cable 13 wires for HD+

0805673265024000016M

12 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: 0805673265024000016M
Device name: Patient cable 13 wires for HD+
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 23, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K0VVY52NXSFDXWFSGM8EM5N5

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

6305016308056732653399
6305016008056732653368
6305016208056732653382
6305012708056732652767
6305016108056732653375
6305011808056732652750
6305013108056732652781
6305014908056732653108
6305015808056732653344
6305013308056732652798
6305015108056732653139
6305015908056732653351