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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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VIVA — 30 UDI-DI variants, MDR (CIZETA MEDICALI S.P.A.)

MD Atlas
CIZETA MEDICALI S.P.A.

Data from EUDAMED, last updated May 31, 2026

VIVA

805618224VIVA140MT

30 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: CIZETA MEDICALI S.P.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805618224VIVA140MT
Device name: VIVA
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: CIZETA MEDICALI S.P.A.
SRN: IT-MF-000028355
Country: Italy
Email: roberto.comina@cizetamedicali.com
Phone: +390297218127

Variants by status

UDI-DI variants

30 UDI-DI variants

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Applied filters

basicUdiUlid01KSHXZ5069N6PFC5NKKVQ67T9

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

34149-113-208032638972611
34149-132-108056182241375
34149-862-208052439247930
34142-113-108052439247169
34142-132-308056182241344

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