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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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Organization name
UDI-DI code
Reference / catalog number

SENSODYNE Rapid Relief Whitening — Class IIa MDR

MD Atlas
Haleon Medical Devices

EUDAMED last updated this device on May 27, 2026

SENSODYNE Rapid Relief Whitening

50596230DP000000000N909P

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Haleon Medical Devices
UDI-DI code: 05054563022592
Reference / catalog number: A1K0000000UN003

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View device family (Basic UDI)

Manufacturer information

Organization name: Haleon Medical Devices
SRN: IE-MF-000002458
Manufacturer status: Active

Related devices

Corsodyl Active Gum Repair Whitening50596230DP000000000M359AOn the market CORSODYL Complete Protection Whitening50596230DP000000000M359AOn the market Corsodyl Intensive Gum Repair Intense Clean50596230DP000000000M359AOn the market Corsodyl Intensive Gum Repair Intense Clean50596230DP000000000M359AOn the market Corsodyl Intensive Gum Repair White & Polish50596230DP000000000M359AOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
If irritation occurs discontinue use.

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Market distribution

Primary placement in Ireland; available across 3 countries total.

Country	On market since	Until
IrelandPrimary placement		Still on market
Malta		Still on market
XI		Still on market

Device identification

Trade name: SENSODYNE Rapid Relief Whitening
UDI-DI code: 05054563022592
Basic UDI-DI: 50596230DP000000000N909P
Reference / catalog number: A1K0000000UN003
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q0199ODONTOLOGY DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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