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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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Anti-Human Lambda Light Chain — 6 UDI-DI variants, IVDR

MD Atlas
DB Biotech, a.s.

Data from EUDAMED, last updated May 31, 2026

Anti-Human Lambda Light Chain

85850389DB039L7

6 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: DB Biotech, a.s.

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 85850389DB039L7
Device name: Anti-Human Lambda Light Chain
Device model: DB 039
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Mar 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: DB Biotech, a.s.
SRN: SK-MF-000051838
Country: Slovakia
Email: dbbiotech@dbbiotech.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMFS1MWSQ3RDA69DHG3P4279

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

DB 039-RTU-1508585038900475
DB 039-108585038900468
DB 039-RTU-708585038900482
DB 039-0.508585038900451
DB 039-0.108585038900437
DB 039-0.208585038900444