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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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MNS 03 — 7 UDI-DI variants, MDR (Hengst SE)

MD Atlas
Hengst SE

Data from EUDAMED, last updated May 23, 2026

MNS 03

4030776MNS03RG

7 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: Hengst SE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4030776MNS03RG
Device name: MNS 03
Device model: Medizinische Gesichtsmaske
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 13, 2021

Manufacturer & authorised representative

Manufacturer

Name: Hengst SE
SRN: DE-MF-000006819
Country: Germany
Email: healthcare@hengst.de

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01FHWTBA7G4553B5SF4X1SHJ97

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

941631800004030776078480
943531000004030776066852
943631000004030776066869
Hengst MNS 0804030776079050
Hengst MNS 08 (2)04030776080391
Hengst MNS 08 (20)04030776079012
Hengst MNS 08 (50)04030776079005