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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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Atemschutzmasken atemious pro — 14 UDI-DI variants, MDR

MD Atlas
Univent Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Atemschutzmasken atemious pro

426068838200125

14 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: Univent Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426068838200125
Device name: Atemschutzmasken atemious pro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Univent Medical GmbH
SRN: DE-MF-000015594
Country: Germany
Email: info@univent-medical.de
Phone: 0049 7720 6099820

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K9Z16NXPY668FAFHE01Z27B7

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

2102 - 01104260688381013
210304260688381037
210204260688381020
2103 - 01104260688381112
2103 - 03104260688381136
2103 - 03004260688381129
210404260688381044
2104 - 01104260688381211
2104 - 03104260688381235
2104 - 03004260688381228
210904260688381099
2109 - 01104260688381310
2109 - 03104260688381334
2109 - 03004260688381327