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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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mint Lesion — 4 UDI-DI variants, MDR (Mint Medical GmbH)

MD Atlas
Mint Medical GmbH

Data from EUDAMED, last updated May 23, 2026

mint Lesion

426049588MINTLESIONSM

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Mint Medical GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426049588MINTLESIONSM
Device name: mint Lesion
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Feb 15, 2023

Manufacturer & authorised representative

Manufacturer

Name: Mint Medical GmbH
SRN: DE-MF-000020202
Country: Germany
Email: info@mint-medical.de
Phone: +49 6221 321 80 0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01G88WDRM2VNV0G7EBGS93NYG6

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

mint Lesion 3.1204260495883120
mint Lesion 3.1004260495883106
mint Lesion 3.904260495880396
mint Lesion 3.1104260495883113