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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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Sabouraud Dextrose Agar +… — 4 UDI-DI variants, IVDR

MD Atlas
GRASO Zenon Sobiecki

Data from EUDAMED, last updated May 30, 2026

Sabouraud Dextrose Agar + Chloramphenicol

590470803020BT100LJ

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: GRASO Zenon Sobiecki

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Device characteristics

ReagentProfessional testingCompanion diagnosticsAnimal tissues / cells

Identity & classification

Basic UDI-DI: 590470803020BT100LJ
Device name: Sabouraud Dextrose Agar + Chloramphenicol
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Dec 11, 2023

Manufacturer & authorised representative

Manufacturer

Name: GRASO Zenon Sobiecki
SRN: PL-MF-000022437
Country: Poland
Email: martyna.olszewska@graso.com.pl
Phone: +48(58)5623021

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HHC7X2WN9YATNJZ8M4SNB22C

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

3020BT25005904708001909
3020BT10005904708001879
3020BT50005904708001916
3020BT20005904708001886