Primus-HD®Yellow
by Eyebright Medical Technology (Beijing) Co., Ltd. 279 variants
Ref AQBXL22,0.0DModel A1UL, AQBXL
Active
CE MDR
Valid until
25 Feb 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69528868B002RZ 06923669276118 | Date4 Dec 2025 | StatusActive |
Certificates
- G70 086359 0019 Active
Technical documentation EU MDR
- Certifier
- TÜV SÜD Product Service GmbH 0123
- Issued
- 26 Feb 2025
- Expires
- 25 Feb 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Preloaded Intraocular Lens System
- Model / Reference
- A1UL, AQBXL, AQBXL22, 0.0D
- Primary DI / UDI-DI
- 06923669276118
- Basic UDI-DI
- 69528868B002RZ
- EMDN Code
- P030102090201 IOLs, APHAKIC, MONOFOCAL, ASPHERIC, HYDROPHOBIC ACRYLIC
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000003041
- Authorised representative
- Lotus NL B.V. NL-AR-000000121
Other devices from Eyebright Medical Technology (Beijing) Co., Ltd.
See all devices from Eyebright Medical Technology (Beijing) Co., Ltd. →
Properties
Other properties (12)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Sutures: 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