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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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Organization name
UDI-DI code
Reference / catalog number

Mosos CTG — Class IIb MDR by NEXUS ASTRAIA B.V.

MD Atlas
NEXUS ASTRAIA B.V.

EUDAMED last updated this device on Apr 17, 2026

Mosos CTG

87202997749MososCTGFE

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NEXUS ASTRAIA B.V.
UDI-DI code: 08720299774933
Reference / catalog number: Software version 13.0

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View device family (Basic UDI)

Manufacturer information

Organization name: NEXUS ASTRAIA B.V.
SRN: NL-MF-000002707
Manufacturer status: Active

Related devices

Mosos CTG87202997749MososCTGFEOn the market Mosos CTG 12.15.XX87202997749MososCTGFEOn the market

Certificates

Certificate health across this manufacturer's portfolio.

2268297CE01Amended
Quality management systemNotified body: 0344Expiry: Jul 1, 2029

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: Mosos CTG
UDI-DI code: 08720299774933
Basic UDI-DI: 87202997749MososCTGFE
Reference / catalog number: Software version 13.0
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Mosos CTG is primarily concerned with the acquisition and display of CTG signals (CTG = Cardiotocograph) and is intended for use in intramural healthcare.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08720299774933

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12080392VARIOUS CHILDBIRTH SUPPORT AND MATERNAL ASSISTANCE INSTRUMENTS - MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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