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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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MIRI® M Chamber — 2 UDI-DI variants, MDR

MD Atlas
Esco Medical Technologies, UAB

Data from EUDAMED, last updated May 31, 2026

MIRI® M Chamber

477904194MIRIMFAMFA

2 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: Esco Medical Technologies, UAB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 477904194MIRIMFAMFA
Device name: MIRI® M Chamber
Device model: MIRI® M-C
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Esco Medical Technologies, UAB
SRN: LT-MF-000010902
Country: Lithuania
Email: support-medical@escolifesciences.com
Phone: +370 37 470 000

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JY5TMG2GM6VX3D2F6RM649FS

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

MIRI® M Chamber04779041940809
MIRI® M Docking station04779041940816