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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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NanoTYPE — 5 UDI-DI variants, IVDR (Omixon Biocomputing Ltd.)

MD Atlas
Omixon Biocomputing Ltd.

Data from EUDAMED, last updated May 24, 2026

NanoTYPE

599956578001TV

5 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class C

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: Omixon Biocomputing Ltd.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 599956578001TV
Device name: NanoTYPE
Device model: NanoTYPE
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Nov 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: Omixon Biocomputing Ltd.
SRN: HU-MF-000003018
Country: Hungary
Email: support@omixon.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J9ND8WQPETNG8KGQND42M9A9

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

NT2411CE05999565781279
NT4x9611CE05999565781323
NT9611CE05999565781316
NT2411v3CE05999565781361
NT9611v3CE05999565781378