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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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GELATO GO — 6 UDI-DI variants, MDR (GELATERIA INTERNATIONAL S.R.L.)

MD Atlas
GELATERIA INTERNATIONAL S.R.L.

Data from EUDAMED, last updated May 31, 2026

GELATO GO

471326484GELATOGOVX

6 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: 471326484GELATOGOVX
Device name: GELATO GO
Device model: Calzatura ortopedica
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 1, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KN4SCPVGNNY6M7SRVX2XJBXZ

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

471326484194904713264841949
471326484195604713264841956
471326484196304713264841963
471326484197004713264841970
471326484198704713264841987
471326484199404713264841994