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Lucovitaal

EUDAMED

Class I (EU MDR)

Ref 3757CE

by PK Benelux BV

Identity

Trade Name
Lucovitaal EUDAMED
Device Name
Lucovitaal oorspray 20ml EUDAMED
Model / Reference
3757CE EUDAMED

Identifiers

Primary DI / UDI-DI
D-3757CETF EUDAMED
Basic UDI-DI
B-3757CETF EUDAMED
EMDN Code
Q03040299 EAR IRRIGATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class I 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 by PK Benelux BV — Class I — 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 9c6ae4b1-3154-43bc-803e-e1b99d5eda6e 61 fields · synced Jun 18, 2026