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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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UREA AGAR BASE (CHRISTENSEN) ISO — 6 UDI-DI variants, IVDR

MD Atlas
Laboratorios Conda S.A.

Data from EUDAMED, last updated May 23, 2026

UREA AGAR BASE (CHRISTENSEN) ISO

843529511110EL

6 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: Laboratorios Conda S.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 843529511110EL
Device name: UREA AGAR BASE (CHRISTENSEN) ISO
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Aug 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: Laboratorios Conda S.A.
SRN: ES-MF-000025575
Country: Spain
Email: alvaro.prieto@condalab.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G94Q0QBCAJ045TEQJDKXKVYD

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

UREA AGAR BASE (CHRISTENSEN) ISO08435295160276
UREA AGAR BASE (CHRISTENSEN) ISO08435295160269
UREA AGAR BASE (CHRISTENSEN) ISO08435295160214
UREA AGAR BASE (CHRISTENSEN) ISO08435295160245
UREA AGAR BASE (CHRISTENSEN) ISO08435295160252
UREA AGAR BASE (CHRISTENSEN) ISO08435295160221