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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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Vlab — 3 UDI-DI variants, MDR (EKOVUK MEDI, s.r.o.)

MD Atlas
EKOVUK MEDI, s.r.o.

Data from EUDAMED, last updated May 23, 2026

Vlab

859421244VLABLF

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: EKOVUK MEDI, s.r.o.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 859421244VLABLF
Device name: Vlab
Device model: 4000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: EKOVUK MEDI, s.r.o.
SRN: CZ-MF-000040403
Country: Czechia
Email: info@pneuven.cz
Phone: +420 773 850 390

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HRVYNEEP8SS34QSWDAB5GP2Z

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

Vlab-200008594212440201
Vlab-400008594212440126
Vlab-Basic08594212440133