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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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Flexicoupler and Jelly Tab Combo Pack — 7 UDI-DI variants, MDR

MD Atlas
Natus Medical Denmark ApS

Data from EUDAMED, last updated May 23, 2026

Flexicoupler and Jelly Tab Combo Pack

5713315NA001085D

7 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: 5713315NA001085D
Device name: Flexicoupler and Jelly Tab Combo Pack
Device model: 011445
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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KC9AG6BDPB9SF4PJMZFTNS6X

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

Flexicouplers05713315011986
Flexicouplers05713315011993
Flexicouplers05713315011702
Jelly Tab Sensor05713315011979
Jelly Tab Sensor05713315011733
Jelly Tab Sensor05713315012006
Jelly Tab Sensor05713315011740