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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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Clinical Product Suite — 2 UDI-DI variants, MDR

MD Atlas
Nexus Enterprise Diagnostics B.V.

Data from EUDAMED, last updated May 31, 2026

Clinical Product Suite

87202997804SUITEJ5

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Nexus Enterprise Diagnostics B.V.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 87202997804SUITEJ5
Device name: Clinical Product Suite
Device model: Variant 1: Clinical Assistant; Variant 2: Clinical Insight
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: May 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: Nexus Enterprise Diagnostics B.V.
SRN: NL-MF-000022846
Country: Netherlands
Email: quality.ed@nexus-nederland.nl
Phone: +31 88 028 71 00

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JW8NY6E2A595S6PF3QSXZWK6

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

N/A08720299780439
N/A08720299780422