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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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ONE BLACK EDITION — 266 UDI-DI variants, MDR (UNIVET LOUPES SPA)

MD Atlas
UNIVET LOUPES SPA

Data from EUDAMED, last updated May 31, 2026

ONE BLACK EDITION

8057147TTL005XT

266 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: 8057147TTL005XT
Device name: —
Device model: ONE 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

266 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS0406ZCP9W74T73G7RBKSRN

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

KKA14113408057147023111
KKA14223408057147023555
KKA14953408057147024392
KKA150733C08057147024880
KKA090734C08057147008491
KKA149334C08057147024422
KKA149434C08057147024408
KKA141534C08057147023265
KKA14243408057147023630
KKA14203408057147023470
KKA092033C08057147008750
KKA085534C08057147008163
KKA170033C08057147028758
KKA09063408057147007777
KKA08583408057147007524
KKA08573408057147007500