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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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LiMAx Breathing Mask — 2 UDI-DI variants, MDR (Humedics GmbH)

MD Atlas
Humedics GmbH

Data from EUDAMED, last updated May 23, 2026

LiMAx Breathing Mask

912008761HUM100088

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: Humedics GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 912008761HUM100088
Device name: LiMAx Breathing Mask
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 27, 2023

Manufacturer & authorised representative

Manufacturer

Name: Humedics GmbH
SRN: DE-MF-000005094
Country: Germany
Email: info@humedics.de
Phone: +49 30 6293955 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H5SBNAHAGCEY0ZVBWPTAW6VR

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

LiMAx Breathing Mask Set A09120087610068
LiMAx Breathing Mask Set B09120087610099