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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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Idocare Visel istuintyyny — 7 UDI-DI variants, MDR (Mekalasi Oy)

MD Atlas
Mekalasi Oy

Data from EUDAMED, last updated May 23, 2026

Idocare Visel istuintyyny

6430074266370VT

7 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: Mekalasi Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6430074266370VT
Device name: Idocare Visel istuintyyny
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 16, 2023

Manufacturer & authorised representative

Manufacturer

Name: Mekalasi Oy
SRN: FI-MF-000003102
Country: Finland
Email: mekalasi@mekalasi.fi
Phone: +358934172800

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H320BFZ8Y1W454RDMBXNDT22

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

28100006430074266370
281038206430074265816
281040206430074265885
281043206430074265953
281046206430074266028
281050206430074266097
281052606430074266165