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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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UNIKO — 12 UDI-DI variants, MDR (Malvestio Spa)

MD Atlas
Malvestio Spa

Data from EUDAMED, last updated May 31, 2026

UNIKO

805830260UNIKOET

12 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: 805830260UNIKOET
Device name: UNIKO
Device model: 326040MC, 326080M, 326080MC, 328019MC, 328059M, 328059MC, 326040M, 326060M, 326060MC 328019M, 328040M, 328040MC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KSMSYD3X0ABF1RR1G9PWG7G4

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

328059M08058302603476
328019M08058302600659
326080MC08058302603452
326060M08058302600284
326040M08058302603490
328040M08058302600666
326080M08058302603445
326040MC08058302603438
326060MC08058302600291
328040MC08058302600673
328019MC08058302603469
328059MC08058302603483