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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 | Number471410212211209001N5 | Date10 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- Withdrawn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/MDR Active
Specification
- Device Name
- 58% Etafilcon A Daily Disposable Soft Contact Lenses50% Toufilcon B Frequent Replacement Soft Contact Lenses38% Polymacon Frequent Replacement Soft Contact Lenses
- Model / Reference
- More
- Primary DI / UDI-DI
- 4714102125000410370BRE, 4714102125042410315BUZ, 4714102125000510312BR7
- Basic UDI-DI
- 471410212211209001N5, 471410212211209019NQ, 471410212211209017NL
- EMDN Code
- Q021004010101, Q0210040102
- Device Class
- Class IIa
- Special Device Type
- Standard soft contact lenses
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- TW-MF-000018739
- Authorised representative
- PEGATRON Czech s.r.o. CZ-AR-000002395
Other devices from Pegavision Corporation
Properties
Other properties (11)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No