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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 ONEHIIRO PRO — 12 UDI-DI variants, MDR

MD Atlas
Univent Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Atemschutzmasken ONEHIIRO PRO

426068838000X43

12 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: 426068838000X43
Device name: Atemschutzmasken ONEHIIRO PRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 26, 2026

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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KMNCBSQECT401E8YXJP22VN5

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

0003 - 01104260688382119
0003 - 01004260688382140
0003 - 03004260688382126
0003 - 00504260688382133
0002 - 01104260688382218
0002 - 01004260688382249
0002 - 03004260688382225
0002 - 00504260688382232
0001 - 01104260688382317
0001 - 01004260688382348
0001 - 03004260688382324
0001 - 00504260688382331