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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 Responder — 3 UDI-DI variants, MDR (Natus Medical Denmark ApS)

MD Atlas
Natus Medical Denmark ApS

Data from EUDAMED, last updated May 23, 2026

Patient Responder

5713315NA000285E

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: Natus Medical Denmark ApS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5713315NA000285E
Device name: Patient Responder
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 19, 2026

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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KHV5GE5GA2A152B1054RY5TW

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

8-31-1900205713315008627
8-31-19005713315000713
8-31-20005713315008610