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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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MASCHERA RILASSANTE MONOUSO — 2 UDI-DI variants, MDR

MD Atlas
ALE & GIO' GROUP SRL

Data from EUDAMED, last updated May 31, 2026

MASCHERA RILASSANTE MONOUSO

805138024TA0304UY

2 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: ALE & GIO' GROUP SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805138024TA0304UY
Device name: MASCHERA RILASSANTE MONOUSO
Device model: TA0304
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: ALE & GIO' GROUP SRL
SRN: IT-MF-000048813
Country: Italy
Email: alexandernicoletti@alegio.it
Phone: +393926935981

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KFJGEBC5Y15DYEQW2AZE8V42

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

TA0308051380241882
TA0408051380241899