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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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ATA 3i Cable Assembly, V.2, CI — 5 UDI-DI variants, MDR

MD Atlas
Natus Medical Denmark ApS

Data from EUDAMED, last updated May 23, 2026

ATA 3i Cable Assembly, V.2, CI

5713315NA001425D

5 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: Natus Medical Denmark ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5713315NA001425D
Device name: ATA 3i Cable Assembly, V.2, CI
Device model: 010726
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: Natus Medical Denmark ApS
SRN: DK-MF-000001617
Country: Denmark
Email: martha.kennedy@natus.com
Phone: +353-91-647433

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KC9EAW05RY37W8DMW4ZHPR3D

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

Algo 3i05713315012242
Algo 3i05713315012235
Algo 3i05713315012211
Algo 3i05713315011726
Algo 3i05713315012228