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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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Medical face mask, type I — 16 UDI-DI variants, MDR (Lifa Air Oy Ltd)

MD Atlas
Lifa Air Oy Ltd

Data from EUDAMED, last updated May 23, 2026

Medical face mask, type I

643007723LM1000UR

16 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: Lifa Air Oy Ltd

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 643007723LM1000UR
Device name: Medical face mask, type I
Device model: LM1000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 22, 2021

Manufacturer & authorised representative

Manufacturer

Name: Lifa Air Oy Ltd
SRN: FI-MF-000002802
Country: Finland
Email: asiakaspalvelu@lifa.net
Phone: +358 9 394 858

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FJKKBW36NASWSGT0JS6BR8NQ

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

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643004369106606430043691066
643007723028606430077230286
643007723020006430077230200
643007723012506430077230125
643007723047706430077230477
643007723048406430077230484
643007723039206430077230392
643007723038506430077230385
643007723046006430077230460
643007723050706430077230507
643007723030906430077230309
643007723031606430077230316
643007723049106430077230491