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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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MRI System — 3 UDI-DI variants, MDR (SternMed GmbH)

MD Atlas
SternMed GmbH

Data from EUDAMED, last updated May 23, 2026

MRI System

42517308007L8

3 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: SternMed GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 42517308007L8
Device name: MRI System
Device model: Marcom 0.35T / Marcom 0.5T / Marcom 1.5T
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 29, 2022

Manufacturer & authorised representative

Manufacturer

Name: SternMed GmbH
SRN: DE-MF-000015421
Country: Germany
Email: info@sternmed.de
Phone: +49 757 35978 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G0C9XZ456J7MZ9B9V4VPE85R

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

116014004251730800293
116016004251730800309
116012004251730800286