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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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AGILE, BRERA, ENTHES, INTHES, ITALA,… — 9 UDI-DI variants, MDR

MD Atlas
Malvestio Spa

Data from EUDAMED, last updated May 31, 2026

AGILE, BRERA, ENTHES, INTHES, ITALA, SISTY

805830260BARMEC66

9 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805830260BARMEC66
Device name: AGILE, BRERA, ENTHES, INTHES, ITALA, SISTY
Device model: 320740, 320750, 320750RX, 320830_E, 320832, 320834, 320760RX, 320760, 320610R
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

9 UDI-DI variants

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Applied filters

basicUdiUlid01KSHTGDWCJ8N0XMZV40VS4H5K

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

32074008058302600161
32075008058302600178
320750RX08058302600185
320830_E08058302600215
32083208058302600222
32083408058302600239
320760RX08058302600208
32076008058302600192
320610R08058302600154