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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 iQ — 11 UDI-DI variants, MDR (B. Braun Avitum AG)

MD Atlas
B. Braun Avitum AG

Data from EUDAMED, last updated May 23, 2026

Dialog iQ

40392390000005292G

11 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: B. Braun Avitum AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 40392390000005292G
Device name: Dialog iQ
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Sep 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: B. Braun Avitum AG
SRN: DE-MF-000005127
Country: Germany
Email: eudamed@bbraun.com
Phone: +49 5661 710

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K5C05NRYHX0R2M8ZJN7G353Q

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

B.Braun04046964447327
B.Braun04046964447334
B.Braun04046964447341
B.Braun04046964447259
B.Braun04046955816415
Dialog iQ®04046955815166
Dialog iQ®04046955815159
Dialog iQ®04046955815203
Dialog iQ®04046955815180
Dialog iQ®04046955815173
Dialog iQ®04046955815197