Reflugel
by So.se.pharm S.R.L. Societa' Di Servizio per L'industria Farmaceut Ica Ed Affini
Ref 660Model Reflugel
Active
CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-08058333980980 08058333980980 | Date24 Jun 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device Name
- Dispositivo medico in sospensione orale per il trattamento dei sintomi da reflusso gastroesofageo
- Model / Reference
- Reflugel, 660
- Primary DI / UDI-DI
- 08058333980980
- Basic UDI-DI
- B-08058333980980
- EMDN Code
- V9099 Various devices not included in other classes - other
- Device Class
- Class IIa
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000042328
Other devices from So.se.pharm S.R.L. Societa' Di Servizio per L'industria Farmaceut Ica Ed Affini
Properties
Other properties (11)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No