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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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NucleoSpin® Dx Blood — 2 UDI-DI variants, IVDR

MD Atlas
MACHEREY-NAGEL GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

NucleoSpin® Dx Blood

4046681151026VX

2 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: MACHEREY-NAGEL GmbH & Co. KG

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 4046681151026VX
Device name: NucleoSpin® Dx Blood
Device model: NucleoSpin® Dx Blood
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jun 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: MACHEREY-NAGEL GmbH & Co. KG
SRN: DE-MF-000005636
Country: Germany
Email: sales@mn-net.com
Phone: +49 2421 9690

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H2WM8Z5039ANB5NZK9471AQH

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

740899.5004046681006302
740899.25004046681006319