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Dicotuss baby med 100 ml IT

EUDAMED

Class IIa (EU MDR)

Ref FTP008

by Labomar S.p.A.

Identity

Trade Name
Dicotuss baby med 100 ml IT EUDAMED
Device Name
Sciroppo Tosse baby EUDAMED
Model / Reference
FTP008 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FTP008EM EUDAMED
Basic UDI-DI
B-FTP008EM 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

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

Dicotuss baby med 100 ml IT 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 29c5c88c-8161-437e-96fc-0baf7c0ad39d 61 fields · synced Jun 18, 2026