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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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ITA35 — 4 UDI-DI variants, MDR (I.T.A.L. S.r.l.)

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

Data from EUDAMED, last updated May 30, 2026

ITA35

8050628388050628381076D2

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.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8050628388050628381076D2
Device name: ITA35
Device model: BUSTO IPERESTENSORE A 3 PUNTI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 13, 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

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Applied filters

basicUdiUlid01J08HK37MQ9EGT0TASQV77KX3

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

ITA 3508050628381243
ITA 3508050628381076
ITA 3508050628381250
ITA 3508050628381236