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.

TECHNE — 970 UDI-DI variants, MDR (UNIVET LOUPES SPA)

MD Atlas
UNIVET LOUPES SPA

Data from EUDAMED, last updated May 31, 2026

TECHNE

8057147TTL006XV

970 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: 8057147TTL006XV
Device name: —
Device model: TECHNE
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

970 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

basicUdiUlid01KS042V3B9C8E4W8YSSM6R5XT

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

KKA24853308057147043362
KKA22843308057147039457
KKA223433C08057147038566
KKA23283308057147040293
KKA04373408057147010593
KKA218233C08057147037583
KKA04913308057147009016
KKA252333C08057147044154
KKA232533C08057147040330
KKA21503408057147036852
KKA02203308057147010661
KKA236033C08057147040996
KKA22573408057147038962
KKA232433C08057147040323
KKA22133308057147038108
KKA22223308057147038276
KKA221533C08057147038160
KKA02103308057147009351
KKA231633C08057147040132
KKA23373308057147040507
KKA235134C08057147040828
KKA23513408057147040767
KKA249534C08057147043584
KKA249634C08057147043652
KKA239734C08057147041689