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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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Lääkitys — 2 UDI-DI variants, MDR (Mediconsult Oy)

MD Atlas
Mediconsult Oy

Data from EUDAMED, last updated May 23, 2026

Lääkitys

6429810579MEDICTNT9

2 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: Mediconsult Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6429810579MEDICTNT9
Device name: Lääkitys
Device model: Lääkitys (Saga)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: Mediconsult Oy
SRN: FI-MF-000008741
Country: Finland
Email: mediconsult@mediconsult.fi
Phone: +358105245500

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JPM3E95879X3SK8VVK9X3GFY

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

Lääkitys (Mediatri)64298105790348
Lääkitys (Saga)64298105790652