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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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Ez RDM (Radiation Dose Monitor) — 3 UDI-DI variants, MDR (MPTronic)

MD Atlas
MPTronic

Data from EUDAMED, last updated May 19, 2026

Ez RDM (Radiation Dose Monitor)

376031406EZRDM9D

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: MPTronic

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 376031406EZRDM9D
Device name: Ez RDM (Radiation Dose Monitor)
Device model: Ez RDM (Radiation Dose Monitor)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 2, 2022

Manufacturer & authorised representative

Manufacturer

Name: MPTronic
SRN: FR-MF-000014183
Country: France
Email: info@mptronic.com
Phone: +33140240830

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FWK66475V5MGV0TSYZW5WAYB

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

Ez RDM03760314060134
Radiation Dose Monitor (RDM)37603140600808
Radiation Dose Monitor (RDM)37603140601270