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 RX — 420 UDI-DI variants, MDR (UNIVET LOUPES SPA)

MD Atlas
UNIVET LOUPES SPA

Data from EUDAMED, last updated May 31, 2026

TECHNE RX

8057147TTL008XZ

420 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: 8057147TTL008XZ
Device name: —
Device model: TECHNE RX
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

420 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

basicUdiUlid01KS046FWDS1XE704VERP33X0E

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

KKA004534C08057147013983
KKA004134C08057147013822
KKA067333C08057147015710
KKA06483408057147012597
KKA071333C08057147015291
KKA022933C08057147014508
KKA02383308057147013457
KKA07023308057147011903
KKA064233C08057147013792
KKA004434C08057147015673
KKA00563408057147012658
KKA06403308057147013501
KKA002934C08057147015611
KKA023833C08057147015024
KKA06863408057147013204
KKA070133C08057147014133
KKA069034C08057147013839
KKA070833C08057147014560
KKA07053308057147013068
KKA026133C08057147015574
KKA06813408057147012238
KKA00503408057147011958
KKA00603408057147012641
KKA00433408057147012153
KKA060934C08057147014966

1 2 3 4 5