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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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Medis Suite MRCT — 1 UDI-DI variant, MDD

MD Atlas
Medis Medical Imaging Systems bv

Data from EUDAMED, last updated May 31, 2026

Medis Suite MRCT

B-B141MEDISSUITEMRCT2025

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Medis Medical Imaging Systems bv

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: BE19/819943785
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: SGS Belgium NV (1639)
Validity: Feb 11, 2024

Identity & classification

Basic UDI-DI: B-B141MEDISSUITEMRCT2025
Device name: Medis Suite MRCT
Device model: 2025
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: Medis Medical Imaging Systems bv
SRN: NL-MF-000002670
Country: Netherlands
Email: bgoedhart@medisimaging.com
Phone: +31715241700

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JV7QZ9Y2VP4Q1JDWR72GKMHP

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

Medis Suite MRCTB141MEDISSUITEMRCT2025