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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 patjat — 33 UDI-DI variants, MDR (Mekalasi Oy)

MD Atlas
Mekalasi Oy

Data from EUDAMED, last updated May 23, 2026

Idocare Visel patjat

6430074264130UP

33 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: 6430074264130UP
Device name: Idocare Visel patjat
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

33 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H31PHEK71MDH172RCRBQTBPC

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

295801306430074267001
285801306430074264765
295851306430074267070
285851306430074264833
295881306430074267148
285881306430074264901
295901306430074267216
285901306430074264970

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