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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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Milieu gélosé — 3 UDI-DI variants, IVDR

MD Atlas
INTELLIGENCE ARTIFICIELLE APPLICATIONS

Data from EUDAMED, last updated May 19, 2026

Milieu gélosé

366662802002DT

3 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: INTELLIGENCE ARTIFICIELLE APPLICATIONS

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 366662802002DT
Device name: Milieu gélosé
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: INTELLIGENCE ARTIFICIELLE APPLICATIONS
SRN: FR-MF-000021688
Country: France
Email: i2a@i2a.info
Phone: +33467504800

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G3XDCX2K5N9H6FGSNHGPENKH

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

Gélose Mueller Hinton - Boite carrée 120 x 120 mm03666628002559
Gélose Mueller Hinton - Boite ronde 90 mm03666628002566
MHR-SIR - Gélose Mueller Hinton Rapide - Boite carré 120 x 120 mm03666628002542