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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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Moistening solution for nasal use… — 2 UDI-DI variants, MDR

MD Atlas
URSAPHARM Arzneimittel GmbH

Data from EUDAMED, last updated May 23, 2026

Moistening solution for nasal use based on sodium hyaluronate

4031626101420N3

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: URSAPHARM Arzneimittel GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4031626101420N3
Device name: Moistening solution for nasal use based on sodium hyaluronate
Device model: Moistening solution for nasal use
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: URSAPHARM Arzneimittel GmbH
SRN: DE-MF-000007748
Country: Germany
Email: erik.seimetz@ursapharm.de
Phone: +49 68 05 92 92 141

Variants by status

UDI-DI variants

2 UDI-DI variants

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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

55.176504031626001887
56.007704031626001719