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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 — 8 UDI-DI variants, MDR (Malvestio Spa)

MD Atlas
Malvestio Spa

Data from EUDAMED, last updated May 31, 2026

ARIA

805830260ARIAAZ

8 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 deviceMeasuring function

Identity & classification

Basic UDI-DI: 805830260ARIAAZ
Device name: ARIA
Device model: 3900B, 3900SB, 3905B, 3905SB, 3960B, 3960SB, 3965B, 3965SB
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 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

8 UDI-DI variants

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Applied filters

basicUdiUlid01KS5DAWQ86VW7K8JGRF2GJPHZ

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

3905B08058302602998
3905SB08058302602950
3965SB08058302602974
3960SB08058302602967
3900SB08058302602943
3965B08058302602578
3900B08058302602981
3960B08058302600086