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Sciroppo Tosse. 150 mL IT

EUDAMED

Class IIa (EU MDR)

Ref FTPR44

by Labomar S.p.A.

Identity

Trade Name
Sciroppo Tosse. 150 mL IT EUDAMED
Device Name
ZERO COUGH FAMILY SYRUP EUDAMED
Model / Reference
FTPR44 EUDAMED

Identifiers

Primary DI / UDI-DI
08056300621348 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
Italy 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

Sciroppo Tosse. 150 mL IT 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 d0bcabae-9c41-48c2-9498-45acaa093565 61 fields · synced Jun 19, 2026