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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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RPMI Agar — 3 UDI-DI variants, IVDR (Reactivos para Diagnóstico)

MD Atlas
Reactivos para Diagnóstico

Data from EUDAMED, last updated May 23, 2026

RPMI Agar

84365422204910SK

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: Reactivos para Diagnóstico

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Device characteristics

Professional testingCompanion diagnostics

Identity & classification

Basic UDI-DI: 84365422204910SK
Device name: RPMI 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01HVTYQXPQZSC63CN31CJQ9NCF

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

RPMI Agar18436542220498
RPMI Agar28436542220495
RPMI Agar84365422204910