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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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FASCIA AUTORISCALDANTE — 6 UDI-DI variants, MDR (ALE & GIO' GROUP SRL)

MD Atlas
ALE & GIO' GROUP SRL

Data from EUDAMED, last updated May 30, 2026

FASCIA AUTORISCALDANTE

805138024NT75813K

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: ALE & GIO' GROUP SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805138024NT75813K
Device name: FASCIA AUTORISCALDANTE
Device model: NT7581
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 20, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KFDKK89ZP3E4VZG47SC5Z1DB

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

NT07508051380241226
NT07808051380241257
NT08108051380241271
NT07608051380241233
NT07908051380241264
NT07708051380241240