Identity
- Trade Name
- NeoBorocillina Sollievo Tosse IT EUDAMED
- Device Name
- NeoBorocillina Sollievo Tosse EUDAMED
- Model / Reference
- FTP051 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-FTP051EN EUDAMED
- Basic UDI-DI
- B-FTP051EN 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
NeoBorocillina Sollievo Tosse 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-FTP051EN | Class IIa | Active |
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Manufacturer
- Manufacturer
- Labomar S.p.A.
- EUDAMED SRN
- IT-MF-000007965
Sources (1)
- EUDAMED 91a1dd0b-e04c-42a3-bb52-ce38c2669dde 61 fields · synced Jun 19, 2026