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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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NeXus-Q32 — 2 UDI-DI variants, MDR (Mind Media Europe B.V.)

MD Atlas
Mind Media Europe B.V.

Data from EUDAMED, last updated May 30, 2026

NeXus-Q32

0871948155NXQ32BZ

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: Mind Media Europe B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0871948155NXQ32BZ
Device name: NeXus-Q32
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: Mind Media Europe B.V.
SRN: NL-MF-000001576
Country: Netherlands
Email: info@mindmedia.com
Phone: +31 475 410123

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GB2SGDJPXKB21QC7VKZZWRDW

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

70-0006-000108719481550363
70-0006-000308719481550394