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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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Mosos CTG — 3 UDI-DI variants, MDR (NEXUS ASTRAIA B.V.)

MD Atlas
NEXUS ASTRAIA B.V.

Data from EUDAMED, last updated May 30, 2026

Mosos CTG

87202997749MososCTGFE

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: NEXUS ASTRAIA B.V.

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Device characteristics

Active device

Legacy certificates

Certificate number: 2268297CE01
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: DEKRA Certification B.V. (0344)
Validity: Mar 24, 2026 → Jul 1, 2029

Identity & classification

Basic UDI-DI: 87202997749MososCTGFE
Device name: Mosos CTG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Jan 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEXUS ASTRAIA B.V.
SRN: NL-MF-000002707
Country: Netherlands
Email: info-nl@astraia.com
Phone: +31 30 666 5021

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JGPDWQDJ37BC91D5FMFAAMWZ

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

Mosos CTG08720299774940
Mosos CTG08720299774933
Mosos CTG 12.15.XX08720299774902