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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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Neumofilt Ergo — 5 UDI-DI variants, MDR

MD Atlas
Medical Respiratory Devices S.L

Data from EUDAMED, last updated May 23, 2026

Neumofilt Ergo

843655723NEUMOFILT3G

5 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: Medical Respiratory Devices S.L

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843655723NEUMOFILT3G
Device name: Neumofilt Ergo
Device model: Neumofilt Ergo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medical Respiratory Devices S.L
SRN: ES-MF-000000824
Country: Spain
Email: hernandez@medicalrd.com
Phone: 916 745 003

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KQS6ZEJP3GB3GVDEPN7GZJW5

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

153608436557230645
153208436557230003
153408436557230324
153508436557230485
153308436557230164