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Apirodent sprej

EUDAMED

Class I (EU MDR)

Ref 1022Model 20 ml

by Apipharma farmaceutsko-prehrambena, kozmetička industrija i trgovina d.o.o.

Identity

Trade Name
Apirodent sprej EUDAMED
Device Name
Apiprodent sprej EUDAMED
Model / Reference
20 ml EUDAMED
1022 EUDAMED

Identifiers

Primary DI / UDI-DI
D-10229G EUDAMED
Basic UDI-DI
B-10229G EUDAMED
EMDN Code
Q019007 BUCCAL TOPICAL TREATMENT PREPARATIONS NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Croatia 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

Apirodent sprej by Apipharma farmaceutsko-prehrambena, kozmetička industrija i trgovina d.o.o. — Class I — MDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
HR-MF-000030055

Sources (1)

  • EUDAMED 820926ef-4cef-4d2b-8f8b-ddb8d58629e2 61 fields · synced Jun 20, 2026