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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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VIVERA MONOBLOC M302 — 4 UDI-DI variants, MDR (MEDIROL s.r.o.)

MD Atlas
MEDIROL s.r.o.

Data from EUDAMED, last updated May 23, 2026

VIVERA MONOBLOC M302

859420773VIVERAM302XB

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: MEDIROL s.r.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 859420773VIVERAM302XB
Device name: VIVERA MONOBLOC M302
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDIROL s.r.o.
SRN: CZ-MF-000006450
Country: Czechia
Email: medirol@medirol.cz

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMQ5M3CGGPV50AD9K50TB0DQ

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

M302V101M0108594207730928
M302V102M0108594207730942
M302V101M0208594207730935
M302V102M0208594207730959