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.

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

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: 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

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

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

KKA091833C08057147008712
KKA150833C08057147024903
KKA14273408057147023753
KKA08913408057147007470
KKA14063408057147022916
KKA085634C08057147008187
KKA143134C08057147023906
KKA142534C08057147023661
KKA09183308057147008019
KKA090634C08057147008477
KKA088233C08057147008705
KKA142234C08057147023548
KKA14173408057147023357
KKA088533C08057147008767
KKA091633C08057147008675
KKA091133C08057147008576
KKA15173308057147025078
KKA08683408057147007722
KKA09123308057147007890
KKA08553408057147007463
KKA15133308057147024996
KKA088833C08057147008828
KKA14233408057147023593
KKA08593408057147007548
KKA089434C08057147008231

5 6 7 8 9