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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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astraia – software for women's health — 4 UDI-DI variants, MDR

MD Atlas
NEXUS / ASTRAIA GmbH

Data from EUDAMED, last updated May 23, 2026

astraia – software for women's health

426074885ASTRAIASC

4 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: NEXUS / ASTRAIA GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426074885ASTRAIASC
Device name: astraia – software for women's health
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 21, 2024

Manufacturer & authorised representative

Manufacturer

Name: NEXUS / ASTRAIA GmbH
SRN: DE-MF-000007042
Country: Germany
Email: info@astraia.com
Phone: +49 89 127 1147-0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FZWQZZM3G59TDTSFSBSZA6RQ

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

29.01.0004260748850022
29.02.0004260748850039
1.27.404260748850008
29.00.0004260748850015