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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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BRILLIANT EverGlow Flow — 10 UDI-DI variants, MDR (Dent4You AG)

MD Atlas
Dent4You AG

Data from EUDAMED, last updated May 23, 2026

BRILLIANT EverGlow Flow

76303929COMP200414K

10 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Dent4You AG

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 76303929COMP200414K
Device name: —
Device model: BRILLIANT EverGlow Flow
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Dent4You AG
SRN: CH-MF-000028926
Country: Switzerland
Email: info.ch@coltene.com
Phone: +41717575300

Authorised representative

Name: Dent4you GmbH
SRN: DE-AR-000006093
Country: Germany
Phone: +49 7345 236540

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KHXKZA0QW3SMJ1WMN65XVA84

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

6001975307630243626588
6001973407630243626557
6001975407630243626595
6001975607630243626618
6001975507630243626601
6001975707630243626625
6001975207630243626571
6001975107630243626564
6002382507630243626649
6001975807630243626632