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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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CLONEXT BLOOD DNA EXTRACTION KIT 200 — 1 UDI-DI variant, IVDR

MD Atlas
Clonit srl

Data from EUDAMED, last updated May 31, 2026

CLONEXT BLOOD DNA EXTRACTION KIT 200

805768091CNextBlood_01CE

1 UDI-DI variant

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: Clonit srl

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 805768091CNextBlood_01CE
Device name: CLONEXT BLOOD DNA EXTRACTION KIT 200
Device model: OP02001-48
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 3, 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

basicUdiUlid01KGJ0M2T701EBV3SGZHACFEEA

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

CLONEXT BLOOD DNA EXTRACTION KIT 20008057680910985