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Organization name
UDI-DI code
Reference / catalog number

Kruidvat Voetschimmel gel — Class IIa MDD by PK Benelux BV

MD Atlas
PK Benelux BV

EUDAMED last updated this device on Apr 30, 2026

Kruidvat Voetschimmel gel

B-073538PB

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: PK Benelux BV
UDI-DI code: D-073538PB
Reference / catalog number: 073538

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View device family (Basic UDI)

Manufacturer information

Organization name: PK Benelux BV
SRN: NL-MF-000006672
Manufacturer status: Active

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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
Keep out of reach of small children. If you are suffering from hypersensitivity reactions, stop using Athlete’s foot gel. Only for external use. Avoid contact with eyes or mucous membranes. Do not apply to open wounds or damaged skin. Consult your doctor when you do not see an improvement within two weeks. No data is available about using Athlete’s foot gel during pregnancy or the breastfeeding period. If you are pregnant or breastfeeding, please consult your doctor or pharmacist before using this product. Possible side effect(s) are redness, itching, stinging or a burning sensation could be adverse effects.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Oct 11, 2021	Still on market

Device identification

Trade name: Kruidvat Voetschimmel gel
UDI-DI code: D-073538PB
Basic UDI-DI: B-073538PB
Reference / catalog number: 073538
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: To support treating fungal infections of the foot (tinea pedis).
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.

M04041503DRESSINGS IN SOLUTIONS, EMULSIONS, GELS, POWDERS WITH SYNTHETIC COMPONENTS

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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