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Unipharma Hoestdrank 2-in-1 120 mL NL

EUDAMED

Class IIa (EU MDR)

Ref FTPR44

by Labomar S.p.A.

Identity

Trade Name
Unipharma Hoestdrank 2-in-1 120 mL NL EUDAMED
Device Name
ZERO COUGH FAMILY SYRUP EUDAMED
Model / Reference
FTPR44 EUDAMED

Identifiers

Primary DI / UDI-DI
08056300621546 EUDAMED
Basic UDI-DI
805630062FTPR449L 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

Unipharma Hoestdrank 2-in-1 120 mL NL 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 a8e6a483-b68c-4b69-af78-37de6e117f5a 61 fields · synced Jul 29, 2026