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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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NemoStudio — 1 UDI-DI variant, MDR (Software Nemotec S.L.)

MD Atlas
Software Nemotec S.L.

Data from EUDAMED, last updated May 31, 2026

NemoStudio

8437023642NemotecSB

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Software Nemotec S.L.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8437023642NemotecSB
Device name: NemoStudio
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Software Nemotec S.L.
SRN: ES-MF-000018790
Country: Spain
Email: carlosarias@nemotec.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSFSZHQRFW09M3PSZ97G385K

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

NemoStudio08437023642085