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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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cNeuro cDAT — 2 UDI-DI variants, MDR (Combinostics Oy)

MD Atlas
Combinostics Oy

Data from EUDAMED, last updated May 23, 2026

cNeuro cDAT

64300708450285

2 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: Combinostics Oy

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Device characteristics

Active device

Legacy certificates

Certificate number: FI22/871878
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: SGS FIMKO OY (0598)
Validity: Oct 11, 2025 → Feb 19, 2030

Identity & classification

Basic UDI-DI: 64300708450285
Device name: cNeuro cDAT
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: Dec 28, 2023

Manufacturer & authorised representative

Manufacturer

Name: Combinostics Oy
SRN: FI-MF-000011968
Country: Finland
Email: contact@combinostics.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HJS1YT26KG2ZPF3NA07B47P2

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

cNeuro cDAT06430070845029
cNeuro cDAT06430070845012