Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Lucovital Athlete's foot spray — Class IIa MDD by PK Benelux BV

MD Atlas
PK Benelux BV

EUDAMED last updated this device on May 1, 2026

Lucovital Athlete's foot spray

B-124254MP

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: PK Benelux BV
UDI-DI code: D-124254MP
Reference / catalog number: 124254

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

View device family (Basic UDI)

Manufacturer information

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

Related devices

RedCare Anti Fusspilz-gelB-17983001CUOn the market ABC Bacterial Vaginosis 5x7 mlB-954854SWOn the market Acetocaustin 2 mlB-073415NSOn the market ActiveMed D-Mannose 28 sB-073156NROn the market Activemed Flacher BauchB-073224NHOn 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
Warnings: • Keep out of reach of small children; • If you are allergic to one of the ingredients or experience an allergic reaction, stop using Athlete’s foot spray; • Only for external use; •Avoid contact with eyes or mucous membranes; • Consult your doctor when you do not see an improvement within two weeks; • The product contains camphor, potentially causing seizures and should be avoided by people with epilepsy • Consult your doctor when you do not see an improvement within two weeks Side effect(s): There are no reported serious side effects. Side effects could be skin irritation such as itching, swelling, rashes and redness. Use during pregnancy and/or breastfeeding: No data is available about using Athlete’s Foot Spray during pregnancy or the breastfeeding period. If you are pregnant or breastfeeding, please consult your doctor or pharmacist before using this product.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Apr 3, 2026	Still on market

Device identification

Trade name: Lucovital Athlete's foot spray
UDI-DI code: D-124254MP
Basic UDI-DI: B-124254MP
Reference / catalog number: 124254
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 the treatment of 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

UDI-DI DataMatrix

D-124254MP

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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

Become a partner of MD Atlas