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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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Nitric Oxide Delivery and Monitoring… — 59 UDI-DI variants, MDR

MD Atlas
INOSYSTEMS

Data from EUDAMED, last updated May 19, 2026

Nitric Oxide Delivery and Monitoring Device

376033338INOTHERAPYEF

59 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: INOSYSTEMS

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 376033338INOTHERAPYEF
Device name: Nitric Oxide Delivery and Monitoring Device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 2, 2022

Manufacturer & authorised representative

Manufacturer

Name: INOSYSTEMS
SRN: FR-MF-000011282
Country: France
Email: contact@inosystems.fr

Variants by status

UDI-DI variants

59 UDI-DI variants

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Applied filters

basicUdiUlid01G9ETTW51BWAMEXFXTRZWRSZP

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

IN00032303760333381074
IN00031603760333381135
IN00033403760333381296
IN00032003760333381098
IN00032203760333381067
IN00033103760333381265
IN00033203760333381272
IN00033803760333381333
IN00033003760333381258

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