Spectacle lenses for Myopia
by Zhejiang Weixing Optical Co., Ltd. 12 variants
Ref 1.76Model 1.50,1.56,1.60,1.67,1.74,PC
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697520819MyopiaQ3 06975208190232 | Date4 Jan 2024 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Spectacle lenses for Myopia
- Model / Reference
- 1.50, 1.56, 1.60, 1.67, 1.74, PC, 1.76
- Primary DI / UDI-DI
- 06975208190232
- Basic UDI-DI
- 697520819MyopiaQ3
- EMDN Code
- Q0210010101, Q0210010102, Q0210010103, Q0210010199
- Device Class
- Class I
- EU market of registration
- Hungary
Manufacturer details
- EUDAMED SRN
- CN-MF-000020605
- Authorised representative
- SUNGO Europe B.V. NL-AR-000000247
Other devices from Zhejiang Weixing Optical Co., Ltd.
Properties
Other properties (13)
- Sterile: No
- 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