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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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Stannous Fluoride 0.454% w/w Occluding… — 7 UDI-DI variants, MDR

MD Atlas
Haleon Medical Devices

Data from EUDAMED, last updated May 24, 2026

Stannous Fluoride 0.454% w/w Occluding Dentifrice

50596230DP000000000N909P

7 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: Haleon Medical Devices

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 50596230DP000000000N909P
Device name: Stannous Fluoride 0.454% w/w Occluding Dentifrice
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Haleon Medical Devices
SRN: IE-MF-000002458
Country: Ireland
Email: slt.consumer-relations@haleon.com
Phone: +44 20 3684 3699

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KRXDQPHTCPBWCD6M87X7KGJX

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

A1K0000000WG01405054563107282
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Sensodyne Rapid Relief Whitening05054563231918
SENSODYNE Rapid Relief Whitening05054563022592
SENSODYNE Rapide Action Blancheur05054563236623