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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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E.L.I.H.A TOXO — 2 UDI-DI variants, IVDR (ELITECH MICROBIO)

MD Atlas
ELITECH MICROBIO

Data from EUDAMED, last updated May 19, 2026

E.L.I.H.A TOXO

3661540PARhemag017C

2 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: ELITECH MICROBIO

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 3661540PARhemag017C
Device name: E.L.I.H.A TOXO
Device model: 66610
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: May 29, 2024

Manufacturer & authorised representative

Manufacturer

Name: ELITECH MICROBIO
SRN: FR-MF-000025235
Country: France
Email: axelle.doctrinal@elitechgroup.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HZ2EKS7SR1CKZZ4ZMEP3Z3P3

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

E.L.I.H.A TOXO03661540100680
TOXO HAI03661540101045