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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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CB240C — 1 UDI-DI variant, MDR (Neuron Guard S.r.l.)

MD Atlas
Neuron Guard S.r.l.

Data from EUDAMED, last updated May 30, 2026

CB240C

805059347COLLAREK

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Neuron Guard S.r.l.

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Device characteristics

Active device

Clinical investigations

Investigation number: 248587
Registered: No
Countries: United Kingdom

Identity & classification

Basic UDI-DI: 805059347COLLAREK
Device name: —
Device model: CB240C
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 16, 2023

Manufacturer & authorised representative

Manufacturer

Name: Neuron Guard S.r.l.
SRN: IT-MF-000027955
Country: Italy
Email: info@neuronguard.com
Phone: +390595801287

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GPX03QJNJ2XPFE7HR5WQ1T94

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

CB240C08050593470041