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

KKA17023308057147028789
KKA08943408057147007531
KKA08963408057147007579
KKA08653408057147007661
KKA14183408057147023395
KKA089134C08057147008170
KKA08973408057147007593
KKA142634C08057147023708
KKA08753308057147007869
KKA08703408057147007760
KKA08883308057147008125
KKA140934C08057147023029
KKA09033408057147007715
KKA087234C08057147008507
KKA089734C08057147008293
KKA15183308057147025092
KKA090334C08057147008415
KKA08833308057147008026
KKA08733408057147007821
KKA14253408057147023678
KKA08903408057147007456
KKA17063308057147028864
KKA14143408057147023234
KKA14923408057147024453
KKA086734C08057147008408