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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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IsoDent Fluor+ hoitava suuvesi 250ml — 2 UDI-DI variants, MDR

MD Atlas
IsoDent Oy

Data from EUDAMED, last updated May 23, 2026

IsoDent Fluor+ hoitava suuvesi 250ml

6430043966430043960278X4

2 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: IsoDent Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6430043966430043960278X4
Device name: IsoDent Fluor+ hoitava suuvesi 250ml
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 25, 2023

Manufacturer & authorised representative

Manufacturer

Name: IsoDent Oy
SRN: FI-MF-000023346
Country: Finland
Email: jyrki.isojarvi@isodent.fi
Phone: +358 407 388 916

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HDM8J77N1X8G8810VX09ECDP

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

643004396035306430043960353
643004396027806430043960278