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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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ARIA — 4 UDI-DI variants, MDR (Malvestio Spa)

MD Atlas
Malvestio Spa

Data from EUDAMED, last updated May 31, 2026

ARIA

805830260ARIANB8J

4 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: Malvestio Spa

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805830260ARIANB8J
Device name: ARIA
Device model: 3905, 3965, 3900, 3960
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Malvestio Spa
SRN: IT-MF-000013307
Country: Italy
Email: info@malvestio.it
Phone: +39 049 9299511

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHXHP22VZMKQPPWSX9AGE0R

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

390508058302602509
396508058302602561
396008058302602554
390008058302602493