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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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surgical mask — 2 UDI-DI variants, MDR (Breckle Matratzenwerk Weida)

MD Atlas
Breckle Matratzenwerk Weida

Data from EUDAMED, last updated May 23, 2026

surgical mask

40194730014D

2 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: Breckle Matratzenwerk Weida

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40194730014D
Device name: surgical mask
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: Breckle Matratzenwerk Weida
SRN: DE-MF-000010222
Country: Germany
Email: information@breckle-weida.de
Phone: +49366030

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FS9RQW3M28P2E7ZMSC35AZ4N

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

BR-MNS 100404019473273121
BR-MNS 100604019473234320