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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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VR VITALIS Pro — 5 UDI-DI variants, MDR (VR LIFE s.r.o.)

MD Atlas
VR LIFE s.r.o.

Data from EUDAMED, last updated May 23, 2026

VR VITALIS Pro

859421497VRVITALISPROU9

5 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: VR LIFE s.r.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 859421497VRVITALISPROU9
Device name: VR VITALIS Pro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: VR LIFE s.r.o.
SRN: CZ-MF-000040304
Country: Czechia
Email: info@vrvitalis.com
Phone: +420 601 581 677

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HR9AE7HJ4XYJCGQM925Y9M25

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

VRP_00508594214970089
VRP_00308594214970065
VRP_00208594214970058
VRP_00108594214970041
VRP_00408594214970072