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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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IgD Immunoglobulins — 2 UDI-DI variants, IVDR (Trimero Diagnostics SL)

MD Atlas
Trimero Diagnostics SL

Data from EUDAMED, last updated May 23, 2026

IgD Immunoglobulins

843447708-IGDCC

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: Trimero Diagnostics SL

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Device characteristics

ReagentProfessional testingHuman tissues / cellsAnimal tissues / cells

Identity & classification

Basic UDI-DI: 843447708-IGDCC
Device name: IgD Immunoglobulins
Device model: 3diag- IgD- TIA Kit
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Feb 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Trimero Diagnostics SL
SRN: ES-MF-000000563
Country: Spain
Email: info@3diag.com
Phone: +34 93 2448679

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JN5ZWPBZF3YXK89YDF4TY78C

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

TD-4265508434477308130
TD-4265008434477208126