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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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VisioFocus — 10 UDI-DI variants, MDR (TECNIMED s.r.l.)

MD Atlas
TECNIMED s.r.l.

Data from EUDAMED, last updated May 30, 2026

VisioFocus

8022386VF064067BZ

10 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: TECNIMED s.r.l.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8022386VF064067BZ
Device name: VisioFocus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: TECNIMED s.r.l.
SRN: IT-MF-000007598
Country: Italy
Email: info@tecnimed.eu

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FQGZREQT0K2WXDH6QFCH32DR

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

0647008022386064775
0640008022386064010
0640008022386064089
0640008022386064065
0671008022386067110
0670008022386067035
0648008022386064805
06480BT08022386064812
0649008022386064829
0647008022386064720