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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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HUMER NEZ BOUCHE - 100% EAU DE MER -… — 3 UDI-DI variants, MDR

MD Atlas
Laboratoires URGO HEALTHCARE

Data from EUDAMED, last updated May 19, 2026

HUMER NEZ BOUCHE - 100% EAU DE MER - SPRAY NASAL

3664492LUHUS0044PM

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: Laboratoires URGO HEALTHCARE

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Device characteristics

Active deviceAnimal tissues / cells

Identity & classification

Basic UDI-DI: 3664492LUHUS0044PM
Device name: HUMER NEZ BOUCHE - 100% EAU DE MER - SPRAY NASAL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: Laboratoires URGO HEALTHCARE
SRN: FR-MF-000001538
Country: France
Email: info@laboratoiresurgo.fr

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HAVVR5K14JYBKKPK2P48RXH5

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

HUMER Blocked Nose hypertonic 100% pure sea water03664492021201
HUMER NEZ BOUCHE03664492023458
366449202114003664492021140