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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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Neon12 — 2 UDI-DI variants, MDR (Incereb Ltd)

MD Atlas
Incereb Ltd

Data from EUDAMED, last updated May 24, 2026

Neon12

539153095TF01KAF

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Incereb Ltd

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 539153095TF01KAF
Device name: Neon12
Device model: TF01K
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 12, 2023

Manufacturer & authorised representative

Manufacturer

Name: Incereb Ltd
SRN: IE-MF-000002463
Country: Ireland
Email: pphillips@incereb.com
Phone: +353 1 685 2245

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HF1PRDSWA5RCW707B9YJD1Y0

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

Neon1205391530950091
TF01-IT05391530950152