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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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MBST Magnetic Resonance Therapy… — 12 UDI-DI variants, MDR

MD Atlas
MedTec Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

MBST Magnetic Resonance Therapy Product Family

40653330MBSTJR

12 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: MedTec Medizintechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 40653330MBSTJR
Device name: MBST Magnetic Resonance Therapy Product Family
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: MedTec Medizintechnik GmbH
SRN: DE-MF-000009592
Country: Germany
Email: info@mbst.de
Phone: +49 (0)641 - 98 46 09-0

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HST96BM6CNY5FQW3DM2QPP9F

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

406533300866204065333008662
406533305117004065333051170
406533300894504065333008945
406533305151404065333051514
406533300746704065333007467
406533300748104065333007481
406533300752804065333007528
406533300754204065333007542
406533300878504065333008785
406533305147704065333051477
406533300846404065333008464
406533300841904065333008419