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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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RespiraSense patient respiratory… — 4 UDI-DI variants, MDR

MD Atlas
PMD Device Solutions Ltd

Data from EUDAMED, last updated May 24, 2026

RespiraSense patient respiratory monitor system.

53915332900RespirasenseDK

4 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: PMD Device Solutions Ltd

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 53915332900RespirasenseDK
Device name: RespiraSense patient respiratory monitor system.
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: PMD Device Solutions Ltd
SRN: IE-MF-000016708
Country: Ireland
Email: info@pmd-solutions.com
Phone: +353 21 242 8760

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01J08QM6QFSKPPQ9JEGNGTZ0Q7

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

RespiraSense05391533290057
RespiraSense05391533290019
RespiraSense05391533290002
RespiraSense App25391533290006