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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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Vytaviteľná krytka — 4 UDI-DI variants, MDR (MARTIKAN s.r.o.)

MD Atlas
MARTIKAN s.r.o.

Data from EUDAMED, last updated May 31, 2026

Vytaviteľná krytka

858602352VKZ6

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: MARTIKAN s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 858602352VKZ6
Device name: Vytaviteľná krytka
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 20, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01KPNEN3VDVAJ7HX64M1DSRCDG

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

VK SVMB 2,608586023525215
VK SVMB 3,6-4,508586023525239
VK-14L08586023525208
VK SVMB 3,008586023525222