Identity
- Trade Name
- Gel Afte. 8 ml IT EUDAMED
- Device Name
- GEL AFTE-LESIONI ORALI EUDAMED
- Model / Reference
- FTP040 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-FTP040_3J6 EUDAMED
- Basic UDI-DI
- B-FTP040_3J6 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
Gel Afte. 8 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-FTP040_3J6 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Labomar S.p.A.
- EUDAMED SRN
- IT-MF-000007965
Sources (1)
- EUDAMED d69460c1-1b0c-47d1-964e-07f9363310dd 61 fields · synced Jun 19, 2026