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Kruidvat (Keelspray / Vaporisateur pour la gorge / Rachenspray) NL/BE

EUDAMED

Class IIa (EU MDR)

Ref FTPR12

by Labomar S.p.A.

Identity

Trade Name
Kruidvat (Keelspray / Vaporisateur pour la gorge / Rachenspray) NL/BE EUDAMED
Device Name
SPRAY GOLA FAMILY EUDAMED
Model / Reference
FTPR12 EUDAMED

Identifiers

Primary DI / UDI-DI
08056300621805 EUDAMED
Basic UDI-DI
805630062FTPR1297 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Kruidvat (Keelspray / Vaporisateur pour la gorge / Rachenspray) NL/BE by Labomar S.p.A. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Labomar S.p.A.
EUDAMED SRN
IT-MF-000007965

Sources (1)

  • EUDAMED 6c910e6e-2403-4fbe-939b-721945c0db55 61 fields · synced Oct 9, 2026