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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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POTATO DEXTROSE AGAR EP/USP/BAM — 4 UDI-DI variants, IVDR

MD Atlas
Laboratorios Conda S.A.

Data from EUDAMED, last updated May 23, 2026

POTATO DEXTROSE AGAR EP/USP/BAM

843529511022EN

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: Laboratorios Conda S.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 843529511022EN
Device name: POTATO DEXTROSE AGAR EP/USP/BAM
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 27, 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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G8ZD6YFYSAYV2GPR0HZZJT0Y

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

POTATO DEXTROSE AGAR EP/USP/BAM08435295164588
POTATO DEXTROSE AGAR EP/USP/BAM08435295164618
POTATO DEXTROSE AGAR EP/USP/BAM08435295164595
POTATO DEXTROSE AGAR EP/USP/BAM08435295164601