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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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Dia-Rinse-CD 3.5 — 5 UDI-DI variants, IVDR

MD Atlas
Diagon Diagnosztikai Korlátolt Felelősségű Társaság

Data from EUDAMED, last updated May 24, 2026

Dia-Rinse-CD 3.5

5992790R03KB

5 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Diagon Diagnosztikai Korlátolt Felelősségű Társaság

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Device characteristics

ReagentProfessional testing

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 5992790R03KB
Device name: Dia-Rinse-CD 3.5
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 24, 2022

Manufacturer & authorised representative

Manufacturer

Name: Diagon Diagnosztikai Korlátolt Felelősségű Társaság
SRN: HU-MF-000023582
Country: Hungary
Email: diagon@diagon.com
Phone: +36 1 369 65 00

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G3TNT9978CE44MA3KR5RB9M8

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

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h1230305992790123036
h3110305992790311037
h2432305992790243239
h1910205992790191028