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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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Noxturnal Web — 2 UDI-DI variants, MDR (Nox Medical)

MD Atlas
Nox Medical

Data from EUDAMED, last updated May 24, 2026

Noxturnal Web

1569431111NOXTURNAL2M

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: Nox Medical

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 1569431111NOXTURNAL2M
Device name: Noxturnal Web
Device model: NOXTURNAL_WEB
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: Feb 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Nox Medical
SRN: IS-MF-000000950
Country: Iceland
Email: support@noxmedical.com
Phone: 354 5707170

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KHBPS0AGGCZ6TMPJP5AB34Z2

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

DeepRESP15694311112129
Noxturnal Web15694311112075