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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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Gluten DQuick DResolution — 1 UDI-DI variant, IVDD (Clonit srl)

MD Atlas
Clonit srl

Data from EUDAMED, last updated May 31, 2026

Gluten DQuick DResolution

B-08057680910688

1 UDI-DI variant

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]IVDD — Annex II List B

Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — Annex II List B
Manufacturer: Clonit srl

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Device characteristics

ReagentProfessional testing

Legacy certificates

Certificate number: 2012 11 0795 CT
Type: refdata.legacy.ivdd-certificate-type.iv-excluding-4-6
Notified body: CENTRO NACIONAL DE CERTIFICACION DE PRODUCTOS SANITARIOS (0318)
Validity: May 26, 2025

Identity & classification

Basic UDI-DI: B-08057680910688
Device name: Gluten DQuick DResolution
Device model: RT-59v3
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — Annex II List B
Version date: Feb 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Clonit srl
SRN: IT-MF-000022196
Country: Italy
Email: info@clonit.it
Phone: +39 0256814413

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KGPGRJQRAZ5WXDCQQGF7PPV2

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

Gluten DQuick Dresolution08057680910688