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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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Class I Ventilator Accessories — 36 UDI-DI variants, MDR

MD Atlas
Breas Medical AB

Data from EUDAMED, last updated May 30, 2026

Class I Ventilator Accessories

7321820139999H

36 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: Breas Medical AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7321820139999H
Device name: —
Device model: Class I Ventilator Accessories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 2022

Manufacturer & authorised representative

Manufacturer

Name: Breas Medical AB
SRN: SE-MF-000001061
Country: Sweden
Email: breas@breas.com
Phone: +4631868800

Variants by status

UDI-DI variants

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G0C0BH7W0R8EFQ9G79GE4TRR

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

00664907321820066490
00634207321820063420
00707907321820070794
00636907321820063697
00785907321820078592
00699807321820069989
00606707321820060672
00626507321820062652
00799907321820079995
00799507321820079957
00599707321820059973

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