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Lucovitaal Keelpijn Zuigtabletten NL

EUDAMED

Class IIa (EU MDR)

Ref FTP087

by Labomar S.p.A.

Identity

Trade Name
Lucovitaal Keelpijn Zuigtabletten NL EUDAMED
Device Name
Gorgewell EUDAMED
Model / Reference
FTP087 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FTP087_4L7 EUDAMED
Basic UDI-DI
B-FTP087_4L7 EUDAMED
EMDN Code
V9017 ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES 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 Keelpijn Zuigtabletten NL by Labomar S.p.A. — 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
Labomar S.p.A.
EUDAMED SRN
IT-MF-000007965

Sources (1)

  • EUDAMED 62bdd46d-cf18-4084-924c-39edc5362e96 61 fields · synced Oct 6, 2026