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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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Deep Breath — 1 UDI-DI variant, MDR (Deep Breath B.V.)

MD Atlas
Deep Breath B.V.

Data from EUDAMED, last updated May 30, 2026

Deep Breath

087208925312123

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Deep Breath B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 087208925312123
Device name: Deep Breath
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Feb 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Deep Breath B.V.
SRN: NL-MF-000044111
Country: Netherlands
Email: dk@deepbreath.tech
Phone: +31642198809

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01JK999TB3C2M6YA2VZEQXGFBA

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

Deep Breath08720892531216