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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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CHROMagar™ Candida — 3 UDI-DI variants, IVDR (CHROMagar™)

MD Atlas
CHROMagar™

Data from EUDAMED, last updated May 19, 2026

CHROMagar™ Candida

376034476CA2276

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: CHROMagar™

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Device characteristics

Animal tissues / cells

Identity & classification

Basic UDI-DI: 376034476CA2276
Device name: CHROMagar™ Candida
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: CHROMagar™
SRN: FR-MF-000024723
Country: France
Email: chromagar@chromagar.com
Phone: +33 1 45 48 05 05

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GSFVH5BSXEHMBP86T2W4BW9D

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

CA223-10kg03760344760028
CA223-2503760344760011
CA22203760344760004