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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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Visia BF 1.50 — 2 UDI-DI variants, MDR

MD Atlas
DIAGONAL d.o.o. za trgovinu i usluge

Data from EUDAMED, last updated May 24, 2026

Visia BF 1.50

385889580ORGLEN150BFCLMC

2 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: DIAGONAL d.o.o. za trgovinu i usluge

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 385889580ORGLEN150BFCLMC
Device name: Visia BF 1.50
Device model: Clear Ophthalmic Bifocal Lens, Index 1.50
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: DIAGONAL d.o.o. za trgovinu i usluge
SRN: HR-MF-000047457
Country: Croatia
Email: vladimir.topic@st.t-com.hr
Phone: 098837851

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JX05MA6Y09JG5VH55V2MGSNE

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

5003858895800086
4603858895800093