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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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LEGIO.mini medical — 3 UDI-DI variants, MDR (LEGIO.tools GmbH)

MD Atlas
LEGIO.tools GmbH

Data from EUDAMED, last updated May 23, 2026

LEGIO.mini medical

42605004430144

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: LEGIO.tools GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42605004430144
Device name: LEGIO.mini medical
Device model: LEGIO.mini medical
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 25, 2023

Manufacturer & authorised representative

Manufacturer

Name: LEGIO.tools GmbH
SRN: DE-MF-000033637
Country: Germany
Email: info@legio.com
Phone: +49-(0)7127-1806-0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HDK7PVX9Z84XS8VVNF96VZGQ

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

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