ProVisc
by Alcon Laboratories, Inc. 11 variants
Ref 0005690103, 0005690036, 0005690012, 0005690102, 0005690020
Active
CE MDR
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/MDR | Number038065GMN000009GV | Date24 Oct 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Provisc Ophthalmic Viscosurgical Device
- Model / Reference
- 0005690103, 0005690036, 0005690012, 0005690102, 0005690020
- Primary DI / UDI-DI
- 00300650569071, 05413895400957, 05413895400780, 00300650569064, 05413895400827
- Basic UDI-DI
- 038065GMN000009GV
- EMDN Code
- Q02030301, Q02030399
- Device Class
- Class IIa
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- US-MF-000016248
- Authorised representative
- Alcon Laboratories Belgium BE-AR-000014721
Other devices from Alcon Laboratories, Inc.
Properties
Other properties (10)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No