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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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UniQueMRIShield — 2 UDI-DI variants, MDR (Arcomed AG)

MD Atlas
Arcomed AG

Data from EUDAMED, last updated May 23, 2026

UniQueMRIShield

764013713-MRI6U

2 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: Arcomed AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764013713-MRI6U
Device name: UniQueMRIShield
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Arcomed AG
SRN: CH-MF-000035749
Country: Switzerland
Email: info@arcomed.com

Authorised representative

Name: Susen Akermann
SRN: DE-AR-000016892
Country: Germany
Phone: +49 151 688 19580

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KGPF6VFR6NBXCYG77C9KP1SM

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

5320-207640137131807
5320-407640137131814