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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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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

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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

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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

KKA18393408057147031994
KKA18813308057147031161
KKA18803308057147031185
KKA18523408057147031734
KKA169633C08057147028673
KKA18423408057147031932
KKA185234C08057147031727
KKA16713308057147028161
KKA187033C08057147031369
KKA168634C08057147028475
KKA156933C08057147026136
KKA185134C08057147031741
KKA188633C08057147031062