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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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VIDIX — 1 UDI-DI variant, MDR (CANFIELD SCIENTIFIC SRL)

MD Atlas
CANFIELD SCIENTIFIC SRL

Data from EUDAMED, last updated May 30, 2026

VIDIX

805317222VIDIXAQ

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: CANFIELD SCIENTIFIC SRL

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 805317222VIDIXAQ
Device name: VIDIX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 15, 2024

Manufacturer & authorised representative

Manufacturer

Name: CANFIELD SCIENTIFIC SRL
SRN: IT-MF-000034524
Country: Italy
Email: michele.bacchion@canfieldsci.com
Phone: 3486803963

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01HPP6C7CDY8XF8ZA9T1XETP7Y

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

VIDIX08053172220013