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Lucovitaal Aambeien Spray

EUDAMED

Class IIa (EU MDR)

Ref 092157

by PK Benelux BV

Identity

Trade Name
Lucovitaal Aambeien Spray EUDAMED
Device Name
Aambeien spray EUDAMED
Model / Reference
092157 EUDAMED

Identifiers

Primary DI / UDI-DI
D-092157PA EUDAMED
Basic UDI-DI
B-092157PA EUDAMED
EMDN Code
M9002 PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS) 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 Aambeien Spray 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 b7172760-b379-4f86-8c8d-f69477ee185c 61 fields · synced Jul 21, 2026