Asqelio™ Pluris Preloaded IOL Delivery System
by AST VisionCare Inc. 69 variants
Ref X2UPIO130Y-V3
Active
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 | NumberB-00840149896832 | Date29 Jul 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- Withdrawn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 Active
Specification
- Device Name
- Asqelio™ Pluris Preloaded IOL Delivery System
- Model / Reference
- X2UPIO130Y-V3
- Primary DI / UDI-DI
- 00840149896832, 00840149897051, 00840149896818, 00840149897273, 00840149897020, 00840149897013, 00840149897112, 00840149897075, 00840149897068, 00840149896870, 00840149896900
- Basic UDI-DI
- B-00840149896832, B-00840149897051, B-00840149896818, B-00840149897273, B-00840149897020, B-00840149897013, B-00840149897112, B-00840149897075, B-00840149897068, B-00840149896870, B-00840149896900
- EMDN Code
- P030102090201 IOLs, APHAKIC, MONOFOCAL, ASPHERIC, HYDROPHOBIC ACRYLIC
- Device Class
- Class IIb
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- US-MF-000021852
- Authorised representative
- MDSS GmbH DE-AR-000005430
Other devices from AST VisionCare Inc.
Properties
Other properties (11)
- 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