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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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Trichomedium — 3 UDI-DI variants, IVDR (GRASO Zenon Sobiecki)

MD Atlas
GRASO Zenon Sobiecki

Data from EUDAMED, last updated May 30, 2026

Trichomedium

590470803042BT100NE

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class C

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: GRASO Zenon Sobiecki

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Device characteristics

ReagentProfessional testingCompanion diagnosticsAnimal tissues / cells

Identity & classification

Basic UDI-DI: 590470803042BT100NE
Device name: Trichomedium
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Dec 20, 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01HJ3MSMA71Y8XVSRDYCGGDK2N

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

3042BT10005904708004597
3042BT50005904708004610
3042BT20005904708004603