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.

ITA BLACK EDITION — 313 UDI-DI variants, MDR (UNIVET LOUPES SPA)

MD Atlas
UNIVET LOUPES SPA

Data from EUDAMED, last updated May 31, 2026

ITA BLACK EDITION

8057147TTL003XP

313 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: UNIVET LOUPES SPA

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: 8057147TTL003XP
Device name: —
Device model: ITA BLACK EDITION
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: UNIVET LOUPES SPA
SRN: IT-MF-000027104
Country: Italy
Email: martina.marzotto@univetloupes.com

Variants by status

UDI-DI variants

313 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

basicUdiUlid01KS03WCT1ER18VK7JTKFJV1D7

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

KKA187833C08057147031215
KKA16973308057147028680
KKA164634C08057147027676
KKA16923308057147028581
KKA11313308057147003137
KKA14913408057147024477
KKA18843308057147031109
KKA18383408057147032014
KKA18583308057147031611
KKA15773308057147026280
KKA165534C08057147027850
KKA188833C08057147031024
KKA149034C08057147024484
KKA15733308057147026204
KKA11003408057147003434
KKA165634C08057147027874
KKA186633C08057147031444
KKA15703308057147026143
KKA112033C08057147003670
KKA11143408057147003373
KKA113033C08057147003731
KKA16723308057147028185
KKA184334C08057147031901
KKA110734C08057147003663
KKA164934C08057147027737

4 5 6 7 8