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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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DialoQ Talk — 2 UDI-DI variants, MDR (Code-Q Oy)

MD Atlas
Code-Q Oy

Data from EUDAMED, last updated May 23, 2026

DialoQ Talk

6429811110DialoQTalk8M

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: Code-Q Oy

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 6429811110DialoQTalk8M
Device name: DialoQ Talk
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: May 3, 2023

Manufacturer & authorised representative

Manufacturer

Name: Code-Q Oy
SRN: FI-MF-000024867
Country: Finland
Email: tapio.koivuniemi@code-q.fi

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GZGMNYEB774NKD3RPCZ7MB8J

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

DLQ-TL06429811110007
DLQ-TLW06429811110014