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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, VIDIX 4.0, VIDIX 4.0 Portatile — 1 UDI-DI variant, MDD

MD Atlas
CANFIELD SCIENTIFIC SRL

Data from EUDAMED, last updated May 31, 2026

VIDIX, VIDIX 4.0, VIDIX 4.0 Portatile

B-80531722200134

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: CANFIELD SCIENTIFIC SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: B-80531722200134
Device name: VIDIX, VIDIX 4.0, VIDIX 4.0 Portatile
Device model: VIDIX, VIDIX 4.0, VIDIX 4.0 Portatile
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Apr 29, 2026

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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Applied filters

basicUdiUlid01KQCSH537B43D3WP674DN4X5Y

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

70071, 7037380531722200134