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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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1081 Madsen A450 — 6 UDI-DI variants, MDR (Natus Medical Denmark ApS)

MD Atlas
Natus Medical Denmark ApS

Data from EUDAMED, last updated May 23, 2026

1081 Madsen A450

5713315NA0004258

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Natus Medical Denmark ApS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5713315NA0004258
Device name: 1081 Madsen A450
Device model: Madsen A450
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KHSP4ME7TF72NSTMJ8C4N25H

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

1081 Madsen A45005713315007248
1081 Madsen A45005713315010309
1081 Madsen A45005713315007224
1081 Madsen A45005713315007231
1081 Madsen A45005713315010323
1081 Madsen A45005713315010316