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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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DIALOG 3.0 — 1 UDI-DI variant, MDR (dialog ausili srl)

MD Atlas
dialog ausili srl

Data from EUDAMED, last updated May 30, 2026

DIALOG 3.0

805759254Y214209DDINCOEFM

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: dialog ausili srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805759254Y214209DDINCOEFM
Device name: DIALOG 3.0
Device model: DIALOG 3.0
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 31, 2022

Manufacturer & authorised representative

Manufacturer

Name: dialog ausili srl
SRN: IT-MF-000022521
Country: Italy
Email: AMMINISTRAZIONE@DIALOGAUSILI.COM
Phone: +393476742552

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01GGPMPHR3ZWFM1N5J1TTKYD0Y

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

DIALOG 3.018057592540130