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Lucovitaal Voetschimmel

EUDAMED

Class IIa (EU MDR)

Ref 064000

by PK Benelux BV

Identity

Trade Name
Lucovitaal Voetschimmel EUDAMED
Device Name
Voetschimmel EUDAMED
Model / Reference
064000 EUDAMED

Identifiers

Primary DI / UDI-DI
D-064000MM EUDAMED
Basic UDI-DI
B-064000MM EUDAMED
EMDN Code
M04041503 DRESSINGS IN SOLUTIONS, EMULSIONS, GELS, POWDERS WITH SYNTHETIC COMPONENTS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Lucovitaal Voetschimmel by PK Benelux BV — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
PK Benelux BV
EUDAMED SRN
NL-MF-000006672

Sources (1)

  • EUDAMED 40be1413-3a1d-4260-941f-ce187d4c69ad 61 fields · synced Jun 19, 2026