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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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Kinos electric treatment tables — 2 UDI-DI variants, MDR (Lojer Oy)

MD Atlas
Lojer Oy

Data from EUDAMED, last updated May 23, 2026

Kinos electric treatment tables

643002193TT0011VN

2 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: Lojer Oy

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 643002193TT0011VN
Device name: —
Device model: Kinos electric treatment tables
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 27, 2023

Manufacturer & authorised representative

Manufacturer

Name: Lojer Oy
SRN: FI-MF-000001639
Country: Finland
Email: info@lojer.com
Phone: +358 10 830 6700

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HB80YGMKR5MZER6C1C8F0GSA

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

Kinos X406430021931542
Kinos X506430021931559