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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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VueBox — 3 UDI-DI variants, MDR (BRACCO SUISSE SA)

MD Atlas
BRACCO SUISSE SA

Data from EUDAMED, last updated May 23, 2026

VueBox

7649996041VueBoxRF

3 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: BRACCO SUISSE SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7649996041VueBoxRF
Device name: VueBox
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 31, 2026

Manufacturer & authorised representative

Manufacturer

Name: BRACCO SUISSE SA
SRN: CH-MF-000022733
Country: Switzerland
Email: vuebox@bracco.com
Phone: +41 22 884 88 84

Authorised representative

Name: ACIST Europe BV
SRN: NL-AR-000002151
Country: Netherlands
Phone: +31652632299

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KMQPXG4CNY3FMCVBNM4R9RJF

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

GI-Perfusion & Liver DVP version 807649996041074
Trial GI-Perfusion & Liver DVP version 807649996041081
VueBox GI-Perfusion Version 807649996041067