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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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SOLE MIO — 8 UDI-DI variants, MDR (GELATERIA INTERNATIONAL S.R.L.)

MD Atlas
GELATERIA INTERNATIONAL S.R.L.

Data from EUDAMED, last updated May 31, 2026

SOLE MIO

471326484SOLEMIOTU

8 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: GELATERIA INTERNATIONAL S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 471326484SOLEMIOTU
Device name: SOLE MIO
Device model: Calzatura ortopedica
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: GELATERIA INTERNATIONAL S.R.L.
SRN: IT-MF-000052928
Country: Italy
Email: info@gelateriainternational.com
Phone: +39 030 6870111

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KMZGTNS4508R5C0AFV98YSXZ

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

471326484795804713264847958
471326484796504713264847965
471326484797204713264847972
471326484798904713264847989
471128194691304711281946913
471128194692004711281946920
471128194693704711281946937
471128194694404711281946944