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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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TECHNE RX BLACK EDITION — 140 UDI-DI variants, MDR (UNIVET LOUPES SPA)

MD Atlas
UNIVET LOUPES SPA

Data from EUDAMED, last updated May 31, 2026

TECHNE RX BLACK EDITION

8057147TTL009Y3

140 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: 8057147TTL009Y3
Device name: —
Device model: TECHNE RX 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

140 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS048E3FB09KAB2GXPBGAAPD

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

KKA125734C08057147017172
KKA12743408057147015901
KKA131733C08057147017219
KKA130433C08057147017110
KKA13053308057147016137
KKA12873408057147016229
KKA13133308057147016380
KKA13013308057147016502
KKA127234C08057147017202
KKA127634C08057147017196
KKA129034C08057147016786
KKA12713408057147016366
KKA128434C08057147016694
KKA13043308057147016267
KKA13143308057147016298

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