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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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1066 MADSEN Astera 2 — 35 UDI-DI variants, MDR

MD Atlas
Natus Medical Denmark ApS

Data from EUDAMED, last updated May 31, 2026

1066 MADSEN Astera 2

5713315NA000385H

35 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: 5713315NA000385H
Device name: 1066 MADSEN Astera 2
Device model: MADSEN Astera 2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 9, 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

35 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K74TZ2363EHT5JG05KWZHR1K

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

8-04-1342005713315010217
8-04-1241605713315010132
8-04-1312105713315007484
8-04-1313105713315006180
8-04-1312405713315007521
8-04-1211805713315007477
8-04-1211505713315007392
8-04-1310405713315007859
8-04-1241805713315010156
8-04-1342405713315010255

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