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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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Coltosol F — 5 UDI-DI variants, MDR (Dent4You AG)

MD Atlas
Dent4You AG

Data from EUDAMED, last updated May 23, 2026

Coltosol F

76303929COMP2009152

5 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76303929COMP2009152
Device name: —
Device model: Coltosol F
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

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

Authorised representative

Name: Coltène/Whaledent GmbH + Co. KG
SRN: DE-AR-000005719
Country: Germany
Phone: +49 7345 805 0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KM0745V027ZZT9VWP0WWG4XT

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

591107630243635948
6004303507630243682225
590607630243635931
6004303407630243682201
6004303607630243682218