Ocu+ 3% Multipack
Ref 5403XModel Ocu+ 3.0% Multipack
Active
CE MDR 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 | Number08500454425400GL 00850045442279 | Date19 Aug 2026 | StatusActive |
| European Union | CE/MDR | Number08500454425400GL 00850045442279 | Date19 Aug 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- Withdrawn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, CE/MDR Active
Specification
- Trade Name
- Ocu+ 3% MultipackOcu+ 3.0% Multipack
- Device Name
- Ocu+ Sterile Viscosurgical DeviceOcu+ Sterile Ophthalmic Viscosurgical Device
- Model / Reference
- 5403X, Ocu+ 3.0% Multipack
- Primary DI / UDI-DI
- 00850045442279
- Basic UDI-DI
- 08500454425400GL, B-00850045442279
- Direct Marketing DI
- 00850045442279
- EMDN Code
- Q02030301 Ophthalmology, hyaluronic acid and derivatives
- Device Class
- Class IIb
- EU market of registration
- GreeceBulgaria
Manufacturer details
- EUDAMED SRN
- US-MF-000013576
- Authorised representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Other devices from Cima Technology, Inc.
Properties
Other properties (12)
- Implantable: No
- 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