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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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m-protect — 3 UDI-DI variants, MDR (qtec CE-Med GmbH)

MD Atlas
qtec CE-Med GmbH

Data from EUDAMED, last updated May 23, 2026

m-protect

426235842CE-MED000001KK

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: qtec CE-Med GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426235842CE-MED000001KK
Device name: m-protect
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: qtec CE-Med GmbH
SRN: DE-MF-000024308
Country: Germany
Email: Hans-Joachim.Graf@qtec-group.com
Phone: +4945180850360

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KMZE8K469YA90X0TNNE611MY

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

MP0033/3404262358420138
MP0028/2904262358420114
MP0031/3204262358420121