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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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NORA — 9 UDI-DI variants, MDR (NORAHEALTH, S.L.)

MD Atlas
NORAHEALTH, S.L.

Data from EUDAMED, last updated May 23, 2026

NORA

8437025841NH013E

9 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: NORAHEALTH, S.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8437025841NH013E
Device name: NORA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Aug 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: NORAHEALTH, S.L.
SRN: ES-MF-000032124
Country: Spain
Email: info@nora.bio

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K220ZPV9TNZYRDMR7BG4BVJV

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

Nora-FR08437025841066
Nora-CT08437025841073
Nora08437025841004
Nora-PT08437025841028
Nora-SI08437025841080
Nora-DE08437025841059
Nora-IT08437025841035
Nora-NL08437025841042
Nora-GB08437025841011