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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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Nuubo System — 3 UDI-DI variants, MDR

MD Atlas
Smart Solutions Technologies, S.L. (NUUBO)

Data from EUDAMED, last updated May 23, 2026

Nuubo System

8437011759NuuboLEONARDOQ2

3 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: Smart Solutions Technologies, S.L. (NUUBO)

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8437011759NuuboLEONARDOQ2
Device name: Nuubo System
Device model: Nuubo Leonardo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 11, 2023

Manufacturer & authorised representative

Manufacturer

Name: Smart Solutions Technologies, S.L. (NUUBO)
SRN: ES-MF-000022284
Country: Spain
Email: info@nuubo.com
Phone: +34 913 60 44 31

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GXR13Y8009X8AVJ7RAXY7Y8T

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

Nuubo System08437011759399
Nuubo System08437011759412
Nuubo System08437011759474