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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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chemagic Pathogen NA gDNA Kit H96 — 3 UDI-DI variants, IVDR

MD Atlas
Revvity chemagen Technologie GmbH

Data from EUDAMED, last updated May 23, 2026

chemagic Pathogen NA gDNA Kit H96

426054336-VBS-H96-BR

3 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: Revvity chemagen Technologie GmbH

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 426054336-VBS-H96-BR
Device name: chemagic Pathogen NA gDNA Kit H96
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Dec 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Revvity chemagen Technologie GmbH
SRN: DE-MF-000017506
Country: Germany
Email: info.chemagen@revvity.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KC4D2T4SRS3FA0C8PFJDTF8Y

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

chemagic Pathogen NA gDNA Kit H9642605433641828
chemagic Pathogen NA gDNA Kit H96 XL42605433642740
Total NA Extraction Kit H9642605433643044