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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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MagSi-DX Pathogen Plus — 4 UDI-DI variants, IVDR (magtivio B.V.)

MD Atlas
magtivio B.V.

Data from EUDAMED, last updated May 31, 2026

MagSi-DX Pathogen Plus

426035032DX0003PL

4 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: magtivio B.V.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 426035032DX0003PL
Device name: MagSi-DX Pathogen Plus
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Mar 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: magtivio B.V.
SRN: NL-MF-000023114
Country: Netherlands
Email: info@magtivio.com
Phone: +31452084810

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQ496D5W89X6YCQSVPCPP6NR

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

MDDX0003009604260350320111
MDDX0003025K04260350320135
MDDX00030005K04260350320128
MDDX0003096004260350320104