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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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GBS Modified Agar — 2 UDI-DI variants, IVDR

MD Atlas
Reactivos para Diagnóstico

Data from EUDAMED, last updated May 23, 2026

GBS Modified Agar

84365422205078SF

2 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: Reactivos para Diagnóstico

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Device characteristics

Professional testingCompanion diagnosticsAnimal tissues / cells

Identity & classification

Basic UDI-DI: 84365422205078SF
Device name: GBS Modified Agar
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 19, 2024

Manufacturer & authorised representative

Manufacturer

Name: Reactivos para Diagnóstico
SRN: ES-MF-000022523
Country: Spain
Email: info-adm@reactivosparadiagnostico.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HVV0S1C9WAK0TFSH6GQY1XM9

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

GBS Modified Agar84365422205078
GBS Modified Agar18436542220504