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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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Reagent — 4 UDI-DI variants, IVDR (LABORATOIRE VERBIESE)

MD Atlas
LABORATOIRE VERBIESE

Data from EUDAMED, last updated May 19, 2026

Reagent

37013999512313SOLQB

4 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: LABORATOIRE VERBIESE

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 37013999512313SOLQB
Device name: Reagent
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: LABORATOIRE VERBIESE
SRN: FR-MF-000023445
Country: France
Email: contact@verbiese.fr
Phone: +33 3 28 50 06 36

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRJPQYEETXACC3W4HKENBQKB

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

512313_3303701399901585
512313_3103701399901608
512313_3203701399901592
512313_3403701399901578