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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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ITALGLOVE - ITALNYTRIL GUANTI IN… — 5 UDI-DI variants, MDR

MD Atlas
I.T.A.L. S.r.l.

Data from EUDAMED, last updated May 30, 2026

ITALGLOVE - ITALNYTRIL GUANTI IN NITRILE MONOUSO SENZA POLVERE

8050628388050628381564DL

5 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: I.T.A.L. S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8050628388050628381564DL
Device name: ITALGLOVE - ITALNYTRIL GUANTI IN NITRILE MONOUSO SENZA POLVERE
Device model: GUANTI MONOUSO IN NITRILE SENZA POLVERE DM- DPI CAT.III
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: I.T.A.L. S.r.l.
SRN: IT-MF-000039832
Country: Italy
Email: rosariadangelo@italortopedia.it

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01J3JM92CVB5M17GRDCJ6Y2AS9

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

INSG1001308050628381564
INSG1001408050628381571
INSG1001508050628381588
INSG1001608050628381595
INSG1001708050628381601