Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

ITALGLOVE - ITALVINYL GUANTI MONOUSO… — 4 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 30, 2026

ITALGLOVE - ITALVINYL GUANTI MONOUSO IN VINILE BLU SENZA POLVERE

8050628388050628381137CV

4 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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8050628388050628381137CV
Device name: ITALGLOVE - ITALVINYL GUANTI MONOUSO IN VINILE BLU SENZA POLVERE
Device model: GUANTI MONOUSO IN VINILE BLU 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 16, 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

4 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01J2XEK99REXSACJCHDG4X9T05

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

IVPG1001408050628381137
IVPG1001508050628381144
IVPG1001608050628381151
www.italortopedia.com08050628381168