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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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MODEL 2 GO — 12 UDI-DI variants, MDR (UNIVET LOUPES SPA)

MD Atlas
UNIVET LOUPES SPA

Data from EUDAMED, last updated May 31, 2026

MODEL 2 GO

8057147TTL015XW

12 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: 8057147TTL015XW
Device name: —
Device model: MODEL 2 GO
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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KS04NFCK7PX2EN6S40V5B6WD

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

KKA25593408057147052067
KKA25463408057147051930
KKA25573408057147052043
KKA25533408057147052005
KKA25403408057147051879
KKA25583408057147052050
KKA25413408057147051886
KKA25513408057147051985
KKA25393408057147051862
KKA25473408057147051947
KKA25453408057147051923
KKA25523408057147051992