Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Neumofilt Ergo Pack Confort — 5 UDI-DI variants, MDR

MD Atlas
Medical Respiratory Devices S.L

Data from EUDAMED, last updated May 23, 2026

Neumofilt Ergo Pack Confort

843655723NEUMOFILTPCRR

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843655723NEUMOFILTPCRR
Device name: Neumofilt Ergo Pack Confort
Device model: Neumofilt Ergo Pack Confort
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 8, 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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KR46BAXHJHD2WENQS71NB1BC

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

1534M08436557230409
1536M08436557230720
1535M08436557230560
1533M08436557230249
1532M08436557230089