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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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Vrták — 5 UDI-DI variants, MDR (MARTIKAN s.r.o.)

MD Atlas
MARTIKAN s.r.o.

Data from EUDAMED, last updated May 31, 2026

Vrták

858602352VMZA

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: MARTIKAN s.r.o.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 858602352VMZA
Device name: Vrták
Device model: VM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: MARTIKAN s.r.o.
SRN: SK-MF-000005834
Country: Slovakia
Email: martikan@martikan.eu

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP5AYHRYYSTJ6A8RS1EM2XTP

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

N 51108586023523990
N 31508586023524003
N 31108586023523969
N 21108586023523976
N 41108586023523983