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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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RADIANTE® 93 Coton — 210 UDI-DI variants, MDR (Radiante SAS)

MD Atlas
Radiante SAS

Data from EUDAMED, last updated May 31, 2026

RADIANTE® 93 Coton

4042809400473229C

210 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Radiante SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4042809400473229C
Device name: RADIANTE® 93 Coton
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Radiante SAS
SRN: FR-MF-000000485
Country: France
Email: EUDAMEDinfo_medical@essity.com

Variants by status

UDI-DI variants

210 UDI-DI variants

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Applied filters

basicUdiUlid01KSJ6VYG9RQ3KJR6D6QVKGCAB

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

73804-00013-0004042809411072
73804-00012-0004042809411065
73800-00008-0004042809412406
73803-00011-0004042809412215
73805-00004-0004042809411188
73835-00001-0004042809406078
73829-00002-0004042809407044
73809-00001-0004042809480672
73831-00008-0004042809406047
73799-00004-0004042809412260

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