Oculade
by S.A.L.F. S.p.A. Laboratorio Farmacologico 16 variants
Ref SIOSV014010Model Oculade
Active
CE MDR
Valid until
19 Jan 2028
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberCSQ0004231724 | Date29 Apr 2026 | StatusActive |
Certificates
- CSQ0004231724 Active
Quality management system EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 29 Apr 2026
- Expires
- 19 Jan 2028
- Reason
- Change approved
- CVD0002230623 Active
Technical documentation EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 29 May 2023
- Expires
- 19 Jan 2028
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- Oculade, SIOSV014010
- Primary DI / UDI-DI
- 08052742101653
- Basic UDI-DI
- 805274210OculadZJ
- EMDN Code
- Q02030301 Ophthalmology, hyaluronic acid and derivatives
- Device Class
- Class III
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000010720
Other devices from S.A.L.F. S.p.A. Laboratorio Farmacologico
See all devices from S.A.L.F. S.p.A. Laboratorio Farmacologico →
Properties
Other properties (11)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No