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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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Dermatophyte Test Agar (Derma TEST Agar) — 2 UDI-DI variants, IVDR

MD Atlas
GRASO Zenon Sobiecki

Data from EUDAMED, last updated May 30, 2026

Dermatophyte Test Agar (Derma TEST Agar)

590470801452PD90PD

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: GRASO Zenon Sobiecki

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Device characteristics

ReagentProfessional testingCompanion diagnosticsAnimal tissues / cells

Identity & classification

Basic UDI-DI: 590470801452PD90PD
Device name: Dermatophyte Test Agar (Derma TEST Agar)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 21, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01HFRRQRH009W98GMB2GSKQBW8

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

1452PD9005904708001091
Dermatophyte Test Agar (Derma TEST Agar)05904708001107